Study Of Treximet, Formerly Known as Trexima, In The Acute Treatment Of Multiple Migraine Attacks
Phase 3
Completed
- Conditions
- Migraine Disorders
- Interventions
- Drug: placebo
- Registration Number
- NCT00240617
- Lead Sponsor
- GlaxoSmithKline
- Brief Summary
The purpose of this study is to determine the consistency of response for Treximet (formerly known as Trexima) when treating four acute migraine attacks at the mild pain phase and within 1 hour of onset of head pain.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 623
Inclusion Criteria
- At least a 6 month history of physician diagnosed migraine and typically experiences 2-6 migraine attacks per month.
- Typically experiences moderate to severe migraine pain preceded by a mild pain phase.
- Differentiate between mild migraine pain and other headache types.
- Women of childbearing potential must be on adequate contraception.
Exclusion Criteria
- Pregnant and/or nursing mother.
- History of cardiovascular disease.
- Uncontrolled hypertension.
- Basilar or Hemiplegic migraine.
- History of stroke or transient ischemic attacks (TIA).
- History of epilepsy or treated with anti-epileptics within past 5 years.
- Impaired hepatic or renal function.
- History of gastrointestinal bleeding or ulceration.
- Allergy or hypersensitivity to Aspirin or any other NSAID.
- Allergy or hypersensitivity to triptans.
- Participated in an investigational drug trial in the previous 4 weeks.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description arm 2 placebo placebo to match arm 1 sumatriptan succinate/naproxen sodium Treximet (sumatriptan/naproxen sodium) formerly known as TREXIMA
- Primary Outcome Measures
Name Time Method Score on a 4 pt migraine pain scale for multiple migraine attacks 2 to 24 hours
- Secondary Outcome Measures
Name Time Method Within patient consistency of response, freedom from all migraine pain and symptoms, satisfaction, presence or absence of neck pain/discomfort, sinus pain/pressure, recurrence of head pain, safety and tolerability 2 to 24 hours
Trial Locations
- Locations (1)
GSK Investigational Site
🇺🇸Wenatchee, Washington, United States