Evaluation of the Efficacy of Diclofenac Potassium and Rimegepant for the Acute Treatment of Migraine
- Sponsor
- Danish Headache Center
- Study ID
- NCT05211154
- Phase
- PHASE4
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Diclofenac Potassium 50Mg/Pkt Oral Pwdr — DRUGTreatment for an acute, moderate to severe migraine attack
- Rimegepant 75 MG — DRUGTreatment for an acute, moderate to severe migraine attack
Study Details
In a real-world population of adults with migraine, the investigators would like to investigate whether 50 mg diclofenac potassium is non-inferior to 75 mg rimegepant in terms of pain freedom at 2 hours after drug intake.
Key Dates
- Start date
- May 5, 2022
- Status verified
- Sep 2025
- Primary completion
- Apr 30, 2025
- Completion
- Apr 30, 2025
Study Design
- Enrollment
- 300 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Diclofenac Potassium (soluble)50 mg diclofenac potassium taken orally once
- Active Comparator: Rimegepant75 mg rimegepant taken orally once
Primary Outcome Measure
Pain freedom at 2 hours [ Time Frame: 2 hours after initial dose ]
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