Comparison of tolerability and efficacy of a combination of paracetamol + caffeine and sumatriptan in the treatment of migraine attack: a randomized, double-blind, double-dummy, cross-over study

Abstract

In this study, we compared the efficacy and tolerability of the combination of paracetamol 1,000 mg + caffeine 130 mg (PCF) with sumatriptan 50 mg (SUM) in migraine attacks. This was a multi-center randomized double-blind, double-dummy, cross-over controlled trial. The efficacy was assessed by the sum of pain intensity differences, the curve of mean pain intensity, the number of pain free at 2 h, and the total pain relief. Tolerability was assessed by recording adverse events within 4 h after drug assumption and evaluating the global judgement of patients. The comparison of these parameters did not show differences between the two drugs which resulted absolutely overlapping in pain relief and patients evaluation. In conclusion, we confirm the efficacy and safety of PCF such as SUM in the treatment of migraine attacks.[PUBLICATION ABSTRACT]

J Headache Pain (2012) 13:669675 DOI 10.1007/s10194-012-0484-z

CLINICAL TRIALS

Comparison of tolerability and efcacy of a combinationof paracetamol + caffeine and sumatriptan in the treatmentof migraine attack: a randomized, double-blind, double-dummy, cross-over study

Luigi Alberto Pini Simona Guerzoni

Michela Cainazzo Michela Ciccarese

Maria Pia Prudenzano Paolo Livrea

Received: 29 July 2012 / Accepted: 2 September 2012 / Published online: 2 October 2012 The Author(s) 2012. This article is published with open access at Springerlink.com

Abstract In this study, we compared the efcacy and tolerability of the combination of paracetamol 1,000 mg ? caffeine 130 mg (PCF) with sumatriptan 50 mg (SUM) in migraine attacks. This was a multi-center randomized double-blind, double-dummy, cross-over controlled trial. The efcacy was assessed by the sum of pain intensity differences, the curve of mean pain intensity, the number of pain free at 2 h, and the total pain relief. Tolerability was assessed by recording adverse events within 4 h after drug assumption and evaluating the global judgement of patients. The comparison of these parameters did not show differences between the two drugs which resulted absolutely overlapping in pain relief and patients evaluation. In conclusion, we conrm the efcacy and safety of PCF such as SUM in the treatment of migraine attacks.

Keywords Migraine Acute treatment

Paracetamolcaffeine combination Sumatriptan

Introduction

Migraine is an intermittent neurological disorder, affecting 1012 % of the western population. In population studies, the prevalence of migraine is approximately 17 % in women and 6 % in men [1]. Migraine is a common, disabling headache disorder, with considerable social and

economic impact, and is currently ranked by the World Health Organization as 19th among causes of years lived with disability [2, 3].

Migraine is diagnosed according to the criteria of the International Headache Society (IHS) as a recurrent headache disorder manifesting with attacks lasting 472 h. Typical characteristics of the migraine headache are unilateral location, pulsating quality, moderate or severe intensity, aggravation by routine physical activity, and association with nausea and/or photophobia, and phonophobia [4].

Acute migraine attacks can be treated with either unspecic drugs such as acetyl salicylic acid and NSAIDs or specic medicines like triptans and ergot alkaloids. In addition, prokinetic drugs and neuroleptics may be useful [57]. Triptans are migraine-specic drugs binding to serotonergic receptors. They are considered rst-line therapy for moderate-severe migraine, or mild-moderate attacks unresponsive to nonspecic analgesics [7]. Triptans are more effective in injectable than in oral formulations and should be avoided in patients with a risk for vascular complication [7]. NSAIDs such as ketorolac and naproxen have the advantage of being appropriate for patients with vascular risk factors and they do not cause sedation [7, 8]. NSAIDs are generally well tolerated and may provide benet even when given late in the migraine attack [8]. However, gastric irritation and occasionally ulceration may complicate treatment with aspirin or other NSAIDs, even when they are used intermittently [7, 8]. The combination of paracetamol and metoclopramide was showed to be superior to paracetamol alone in migraine [9], Paracetamol ? caffeine is an useful alternative to NSAID for tension-type headache (TTH); it was compared with placebo in three high-quality studies, showing its superiority over placebo as well as a good tolerability [10, 11].

Till date there is only a large-scale study comparing the early treatment of an association of migraine of

L. A. Pini S. Guerzoni M. Cainazzo M. Ciccarese

Headache Study Center, University of Modena & Reggio Emilia, Modena, Italy

M. P. Prudenzano (&) P. Livrea

Headache Center, L. Amaducci Neurological Clinic, University of Bari, Bari, Italye-mail: [email protected]

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sumatriptan 50 mg and a combination of aspirin ? acetaminophen ? caffeine [12]. This study has been discussed by some authors for some methodological criticisms [13, 14]. Studies comparing paracetamol ? caffeine versus sumatriptan at low dose for the treatment of mild-severe migraine treatment are lacking.

The aim of this study was to evaluate the association of paracetamol 1,000 mg ? caffeine 130 mg (PCF) to treat acute migraine attacks and compare the efcacy and safety of this product with a gold standard sumatriptan 50 mg by mouth.

Patients and methods

Patients

This multi-center study was conducted between May 2011 and April 2012 in two Italian Headache Centers recruiting 108 outpatient volunteers of both genders (one-third male, age 1862) with a clinical history of episodic migraine fullling the following inclusion criteria:

Diagnosis of migraine fullling ICHD-II criteria for migraine with or without aura.

Mean frequency of 28 attacks per month. If female, adequate contraception in women of fertile age.

Daily consumption of at least two cups of coffee. Medical history and clinical parameters inconsistent with organic or psychiatric disorders associated with headaches.

Exclusion criteria were:

Declared hypersensitivity or allergy to paracetamol or sumatriptan.

Presence of chronic migraine or headache, or medication overuse headache.

Post-traumatic headache. Past or present earth ischemia or myocardial infarction, cerebral ischemic attacks, peripheral vascular diseases, hepatic or renal diseases, mail, severe or uncontrolled hypertension, phenylketonuria, hemolytic anemia.

Treatment with anticoagulants or antiplatelet drugs. Drugs and alcohol abuse, or psychiatric diseases. Coagulation disorders, peptic ulcer disease, pancreatic disease, clinically signicant renal or hepatic disease, blood hypertension, mild/moderate kidney or liver failure, Gilberts syndrome.

The study was conducted, following good clinical practice standards and in accordance with the Declaration of Helsinki (Tokyo version 2004) and stated after independent ethics committee approval for each investigator

(Paracaf-emi-010 Code EudraCt 2010-019083-36). Prior to enrolment the patients gave their written informed consent; they were allowed to terminate participation in the trial at any time, without giving reasons. This trial complies with the guidelines for trials of drug treatments in migraine of the IHS [15].

Study design and treatments

Primary objectives of the study were to show the efcacy of the association of paracetamol 1,000 mg and caffeine 130 mg in reducing pain in migraine attacks, and the tolerability of this combination in migraine treatment. Secondary objective was to demonstrate the non-inferiority of the PCF association versus SUM in a comparison between these two treatment in migraine attacks.

This was a phase IV study randomized, double-dummy, cross-over, drug-controlled trial. We decided to exclude placebo due to some ethical reasons: this a phase IV study, comparing two well-known active drugs, and our ethical committee did not allow private patients of an active treatment in a study aimed to compare two active drugs.

After obtaining the signature on the informed consent form, the patients were required to treat three subsequent consecutive migraine attacks with the investigational study medications, according to a randomized cross-over sequence computer generated using Microsoft_Access 2003. Each patient was randomly allocated to assume either one PCF and two SUM, or two PCF and one SUM in a randomized sequence treatment. Eligible patients were assigned in sequential order of entry. Access to the randomisation code was strictly controlled and the treatment assignment remained unknown to all parties involved in the trial until database formal lock.

Subjects in all treatment groups received three identical boxes (numbered progressively from 1 to 3, to indicate the exact order in which they should have been used) containing: one soft gel capsule containing one tablet of placebo or sumatriptan 50 mg and one sachet containing paracetamol 1,000 mg ? caffeine 130 mg or one sachet containing the excipients and avor as the active drug.

Blinding was ensured using matched trial supplies, identical in color, size, shape, and taste. At each migraine attack patients would have to take one soft gel capsule and one sachet at the same time. The trial medication was to be taken when the headache occurred, and when the patients would normally have taken their usual analgesic. Other than study medication, patients received rescue medication (usual medication for each patient), to be taken 3 h after the administration of the trial medication, if the pain lasted over the 2 h.

At baseline visit, a complete patients medical history and concomitant treatments were recorded, vital signs were measured, and a physical examination was performed by

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the investigator. Patients were required to record in a headache diary, the date and time of drug ingestion, pain intensity before treatment, pain intensity, pain relief, and adverse events (AEs) after treatment recorded at 1, 2, 3, 4, and 24 h. At the end of 4-h measurement interval or at the time of use of rescue medication, the patients had to record the presence and intensity of AEs. A global judgment of the treatment was also required. The same procedures were repeated for the two subsequent migraine attacks.

Outcomes

Safety and tolerability were evaluated by comparing vital signs at screening and nal visits and by recording AEs. AEs could be recorded by the investigator or by the patient lling in a symptom check-list (including nervousness, palpitation, insomnia, dizziness, abdominal pain, dyspepsia, nausea, vomiting, drowsiness, and fatigue) hourly for 4 h after the study medication ingestion. AEs severity was determined by subjective evaluation of the patient and classied as mild (signs or symptoms easily tolerated), moderate (discomfort sufcient to cause interference with normal activities), and severe (incapacitating with inability to do work or undertake normal activity).

A global assessment of tolerability was expressed by the patient, using a 5-point verbal rating scale (VRS: excellent, very good, good, sufcient, and poor).

To assess treatments efcacy, intensity of pain (on a 4-point scale: 0 absent, 1 mild, 2 moderate, 3 severe) and pain relief (on a 5-point scale: 0 no relief, 1 little relief, 2 some relief, 3 much relief, 4 complete relief) were evaluated hourly during the 4-h post-dose period.

Based on these two variables, the following parameters were calculated:

For each patients the sum of pain intensity differences (SPID) was calculated as the sum of differences between pre-dose assessment and every post-dose assessment.

Total pain relief (TOTPAR), calculated as the sum of every post-dose assessment.

Statistical analysis

Migraine is a disease with a large inter-individual variability to treatment; to reduce this bias the trial is conducted following a double-blind controlled double-dummy cross-over study versus an active drug.

The study was powered to test the primary hypothesis, namely that paracetamol 1,000 mg ? caffeine 130 mg would be non-inferior to SUM as regards the proportion of patients within the 4-h post-dose period.

Assuming a reduction of pain intensity, calculated in a 4-point scale, as recommended by IHS, within 4 h as1.2 1.3 (SD) in the control study group, we assumed that PCF will be non-inferior when the mean will be D = 0.5.

Giving an unilateral a = 0.025 and a 80 % power 110 case for treatment will be enough for statistical analysis.

According to study protocol all the randomized patients who took at least one of the treatments (intention-to-treat, ITT) were evaluated.

Data missing for any scheduled evaluation was replaced by the last observation carried forward (LOCF) procedure. The tolerability endpoints were evaluated using ITT populations; ITT population was employed for efcacy analyses. Descriptive statistics on population was used for demographic and baseline characteristics.

The Fisher exact test (with a 90 % condence interval) was used to compare the percentage of patients who recorded AEs after each treatment. Besides those recorded by patients in the 4-h post-dose period, all the AEs were classied by the investigator on the basis of treatment received, system involved, severity, and correlation with the investigational medication. The analysis of variance was used to evaluate the differences of vital signs respect to baseline.

The analysis of variance was used to evaluate SPID and TOTPAR. The patient preference for one of the treatments was reported as a distribution of frequency. Other statistical tests were used when appropriate.

Results

108 caucasian patients participated in the study and 92 took at least one of the treatment, whereas 16 patients who lled inclusion criteria did not take any medication. In three cases, the subjects in the following days after randomization explicitly refused to continue the study; In the other 13 cases, when the patients where recalled after 2 months for the second scheduled visit, they refused to continue the protocol for personal reasons. Two patients assumed one treatment and eight subjects assumed two treatments; so the ITT population was of 92 cases and were evaluated for efcacy and tolerability for both the treatments. Globally 264 migraine attacks were evaluated, 131 treated with PCF and 133 treated with SUM. The demographic characteristics and headache history of the patients are summarized in Table 1.

With regard to the familial history, 66 (72 %) of cases referred a rst-order relative suffering from headache.

Efcacy

The comparison between the two treatments did not show any difference in pain intensity at baseline both as absolute values and for a Chi square test (p = 0.72).

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Table 1 Demographic data and headache history (ITT, n = 92)

Male 31 (33.6 %)

Female 61 (66.3 %)

Age (years)(mean SD)

Male 33.6 10.5

Female 35.6 9.6

Headache Index 4 3.5

Usual pain intensity

Mild 20 (22 %)

Moderate 49 (53 %)

Severe 23 (25 %)

BMI \18.5 18.524.9 25.029.9 [30 Male (%) 46.2 46.2 7.7

Female (%) 5.9 78.4 11.8 3.9

Headache index = number of day with headache in the observed period

Pain intensity = in a 03 scale

Fig. 1 Time course of pain intensity. In both treatment groups since at time T = 1 h in both groups there was a highly signicant difference versus basal time (paired t test: p \ 0.0001)

Table 2 Sum of pain intensity differences (SPID) and total pain relief (TOTPAR) in the 4-h observation period for the ITT dataset (n = 264)

PCF SUM All t test

SPID

Baseline intensity 2.1 0.7 2.1 0.8 2.1 0.8

Mean SD 3.2 3.8 3.2 3.7 3.2 3.8 p = 0.88 TOTPAR

Mean SD 7.0 3.6 7.4 3.6 7.2 3.6 p = 0.48

SD standard deviation

ANOVA for SPID and TOTPAR showed a positive independent signicant variable for intensity of headache at baseline (p \ 0.001), while no difference between type of treatment (p = 0.8849)

Fig. 2 Time course of the total pain relief (TOTPAR) in the ITT dataset. In both treatment groups, since time T = 01 h there was a highly signicant difference versus basal time (paired t test: p \ 0.0001)

Figure 1 reports the time course of mean pain intensity for PCF and SUM treatment, while the sum of SPID and the TOTPAR in the T 04 h period is illustrated in Table 2.

Data showed that both the treatments are effective with respect to the baseline, but there were no differences between the treatments.

The time course of TOTPAR is reported in Fig. 2, where similar results are showed. Rescue medication was assumed in 38 % of PCF treatments and 45 % of SUM treatment, without signicant differences (Fisher exact test: p = 0.3308), even looking at the timing of assumption, i.e., before or 3 h after the rst treatment (Fisher exact test: p = 0.2245).

Safety

Taking into account the ITT population and the 264 considered attacks, the number of side effects is reported in Table 3. In about half of recorded attacks, we did not register adverse events (0.9 1.2 and 1.1 1.3 for PCF and SUM, respectively), without differences between the treatments (t test: p = 0.156). The intensity of side effects was always slight or moderate, all side effects disappeared spontaneously and none requested any modication of scheduled treatment. The only difference between the treatments was a slight increase of referred fatigue in patients assuming SUM.

In Table 3 the global assessment of efcacy and tolerability is referred as reported by patients. In Table 4 the number of side effects is reported, and in Table 5 the types of side effects recorded are reported.

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Table 3 Assessment of efcacy and tolerability for each treatment (n = 264)

PCF, n (%) SUM, n (%)

Efcacy

Complete relief 97 (74.1) 96 (72.2)

Much relief 8 (6.5) 9 (6.7)

Some relief 7 (5.3) 8 (6.1)

Little 8 (6.5) 9 (6.7)

No relief 11 (8.4) 11 (8.3)

TolerabilityExcellent 53 (40.4) 48 (36.4)

Very good 34 (26.2) 33 (24.6)

Good 16 (12.2) 24 (17.8)

Sufcient 17 (12.8) 15 (11.5)

Poor 11 (8.4) 13 (9.7)

Fisher exact test p = 0.98 for efcacy and p = 0.43 for tolerability

Discussion

Migraine is a widespread condition that in the majority of cases is self-treated by patients, so the use of safe and effective drugs is a reasonable basis for selecting medicines.

Many studies have been conducted to show the efcacy of combination drugs in the treatment of migraine attacks [12, 16, 17].

In a three double-blind, randomized, parallel-group, single-dose, placebo-controlled studies Lipton showed that the combination of acetaminophen, aspirin, and caffeine was highly effective for the treatment of migraine headache pain as well as for alleviating the nausea, photophobia, phonophobia, and functional disability associated with migraine attacks. This drug combination also has an excellent safety prole and is well tolerated [16].

In 2005, Goldstein compared a combination of non-prescription migraine medication (acetaminophen 500 mg, aspirin 500 mg, and caffeine 130 mg) with a prescription migraine product (50 mg sumatriptan) in a randomized, controlled clinical trial in which subjects were treated at the rst sign of a migraine attack. He concluded that the combination of acetaminophen, aspirin, and caffeine was signicantly more effective (p [ 0.05) than sumatriptan in the early treatment of migraine, as shown by superiority in summed pain intensity difference, pain relief, pain intensity difference, response, sustained response, relief of associated symptoms, use of rescue medication, disability relief, and global assessments of effectiveness [12].

More recently Diener [17] in a post hoc analysis reported that the xed combination of ASA (250 mg), paracetamol (200 mg), and caffeine (50 mg) is effective and well tolerated in a broad spectrum from mild-to-severe

migraine and TTH severity independent of the headache diagnosis.

Prior conrmed in a double-blind study that acetaminophen 1,000 mg is an effective and well-tolerated treatment for episodic and moderate migraine headache. In addition, acetaminophen generally provided a benecial effect on associated symptoms of migraine including nausea, photophobia, phonophobia, and functional disability [18].we some years ago, conrmed the efcacy of the acetaminophen ? caffeine association in TTH [11].

In fact, paracetamol exerts its analgesic activity through a direct effect on the central nervous system [19], at least in part mediated by the serotonergic system [20, 21]. Due to its scarce inhibition of peripheral cyclooxygenase: it is better tolerated at gastrointestinal level than NSAIDs, it is only a weak inhibitor of platelets aggregation and does not alter the bleeding time [22].

The association with caffeine is relevant because of the well-known antagonism of adenosine A(2A) and A(2B) receptors, as well as the inhibition of cyclooxygenase activity at some sites, may explain intrinsic antinociceptive and adjuvant actions. When combined with morphine, caffeine can augment, inhibit or have no effect depending on the dose, route of administration, nociceptive test, and species. Low doses of caffeine given systemically inhibit antinociception by several analgesics (acetaminophen, amitriptyline, oxcarbazepine, cizolirtine), probably reecting block of a component of action involving aden-osine A(1) receptors. Clinical studies have demonstrated adjuvant analgesia, as well as some intrinsic analgesia, in the treatment of headache conditions, but not in the treatment of post-operative pain [23], and Diener [24] showed the superiority of the combinations containing caffeine over the association of aspirin and paracetamol alone.

Because the cross-over there were no differences between groups, but it was interesting to note that males showed a BMI signicantly superior to the females (Fisher exact test: p \ 0.001).

Comparing the two treatments, there was a complete overlapping in the efcacy items both for SPID and TOTPAR.

Analyzing the time course of the mean of pain intensity it is interesting to note that at the 24 h almost all patients had resolved their migraine attacks, whereas 41 % of them should assume a rescue medication.

Rescue medication was assumed within both treatments without differences, even when we compared the time of assumption: in fact, there was a small and non-signicant difference between SUM treatment where patients assumed in the 38 % of cases the rescue drug at the time 3 versus a 21 % of assumption in PCF treatments (Fisher exact test: p = 0.22).

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The evaluation of efcacy and tolerability in the patients report again showed a complete equivalence of the treatments. In addition, about 80 % of patients for each treatment declared much or complete relief, and a similar percentage referred a very good/excellent tolerability. Even this parameter did not show the differences between the treatments.

We reported the number of total side effects (Table 4) and the more frequent types in Table 5. In this table, there was a signicant increase of fatigue in patients assuming SUM compared with cases assuming PCF: This datum result isvery low in the PCF treatment whereas the % in the SUM treatment is similar to the placebo group in our previous study [11].

In conclusion, this trial could have relevant implications for the clinical practice, showing that the simple combination of paracetamol 1,000 mg ? caffeine 130 mg seems to be as efcient and safe as sumatriptan 50 mg by mouth, and this could be an important indication for patients suffering from migraine who cannot assume triptans.

Acknowledgments This work was supported by a grant from the Italian League of Cephalalgic Patients (LIC-Onlus) a no-prot association of patients.

Conict of interest PLA received honoraria for participation in clinical trials, contribution to advisory boards, or oral presentations from: Allergan, Almirall, ACRAF, GlaxoSmithKline, Janssen-Cilag, Guidotti, Pzer. The other authors did not have conict of interest with pharmaceutical farm possibly involved to this argument.

Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

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Table 4 Number of adverse events recorded after drug assumption (dataset = 92 patients and 264 treatments)

Adverse events Total Treatments

PCF SUM

N % N % N %

0 (none) 125 47.3 69 52.7 56 42.1

1 72 27.2 32 24.5 40 30.1

2 40 15.1 18 13.6 22 16.5

3 10 3.9 4 2.7 6 4.5

4 14 5.3 8 6.4 6 4.5

5 2 0.8 2 1.6

6 1 0.4 1 0.7

Total 264 100.0 131 100.0 133 100.0

t test: p = 0.156, between treatments

Table 5 Types of adverse events reported by patients (N = 92; 264 treatments)

Total(n = 264)

Treatment Fisher exact test (p)

PCF(n = 131)

SUM(n = 133)

N % N % N %

None 125 47.3 69 52.7 56 42.1

Nervousness 32 12.2 13 10.0 19 14.3 0.4125

Palpitazion 27 10.4 12 9.1 15 11.6 0.6607 Insomnia 11 4.1 6 4.5 5 3.6 0.7471

Dizziness 12 4.5 4 2.7 8 6.3 0.3326

Abdominal pain 12 4.5 3 1.8 9 7.1 0.1016

Dyspepsia 21 8.1 11 7.4 12 8.9 0.8067

Nausea 67 25.2 37 28.2 30 22.3 0.3553

Vomito 6 2.3 4 2.7 2 1.8 0.6818

Drowsiness 42 15.8 18 13.6 24 17.9 0.4625

Fatigue 27 10.4 7 5.5 20 15.1 0.0260

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