Phase 4
Completed N=752
Efficacy and Safety of Acetaminophen, Aspirin and Caffeine With Sumatriptan in the Acute Treatment of Migraine
Pain, Migraine
Source: ClinicalTrials.gov NCT01248468 ↗
Enrolled (actual)
752
Serious AEs
0.0%
Results posted
Jul 2012
Primary outcomePrimary: Percent of Subjects Who Are Pain Free at 2 Hours. — 34.7; 44.9; 26.4 Percent of participants
Summary
The main purpose of this study is to compare the efficacy and safety of aspirin, acetaminophen and caffeine (AAC) with sumatriptan and placebo in the acute treatment of migraine.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percent of Subjects Who Are Pain Free at 2 Hours. |
34.7; 44.9; 26.4 | — |
| SECONDARY Percent of Subjects Who Are Free of Nausea at 2 Hours. |
70.6; 72.2; 66.4 | — |
| SECONDARY Percent of Subjects Who Are Free of Phonophobia at 2 Hours. |
53.4; 60.9; 46.2 | — |
| SECONDARY Percent of Subjects Who Are Free of Photophobia at 2 Hours. |
48.6; 52.3; 40.8 | — |
Eligibility Criteria
Inclusion criteria
- Male or female aged 18 years and over.
- International Headache Society (IHS) diagnosis of migraine without aura or typical aura with migraine headache.
- History of experiencing at least 1, but not more than 8, acute migraine attacks monthly during the previous year.
- History of at least moderate migraine pain intensity, if left untreated.
Exclusion criteria
- Headache symptoms which may be due to or aggravated by:
- Recent (within 6 months) head or neck trauma (e.g., whiplash)
- Head or neck pain secondary to an orthopedic abnormality
- Cluster headache
- Specific migraine variants (e.g., basilar-type artery migraine, ophthalmoplegic migraine, hemiplegic migraine, migraine aura without headache)
- Other serious, non-migraine causes of headache (e.g., increased intracranial pressure, intracranial bleeding, meningitis, malignancy)
- Non-serious, non-migraine causes of headache (e.g., cold, flu, hangover)
- Routine use (≥ 10 days per month, on average) of any medication having the potential to interfere with the pharmacologic effects or evaluation of the study medications (e.g., narcotic and non-narcotic analgesic products (prescription or over-the-counter), ergotamine-containing and ergot-type medication, anxiolytics, hypnotics, sedatives, 5HT-1 agonists, anti-emetics, or prokinetic drugs).
- History of vomiting during more than 20% of migraine episodes or confined to bedrest for more than 50% of migraine episodes.
Other protocol-defined inclusion/exclusion criteria may apply
Data sourced from ClinicalTrials.gov (NCT01248468). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.