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Nonsteroidal Anti-inflammatory Drug (NSAID)
Topical, intra-oral ketoprofen gel for Migraine
Phase 3
Waitlist Available
Led By Caren Behar, MD
Research Sponsored by Behar, Caren, M.D.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 240 minutes post-treatment
Awards & highlights
Study Summary
The purpose of this study is to evaluate the efficacy and safety of intra-oral topical ketoprofen for the treatment of acute migraine.
Eligible Conditions
- Migraine
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within 240 minutes post-treatment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 240 minutes post-treatment
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pain relief (defined as at least 2 graded reduction in a 5-grade scale) at 120 minutes post-treatment
Secondary outcome measures
Need for Rescue Medication between the time of dosing to 240 minutes
Pain free status at 30, 60, 120, and 240 minutes post-treatment based on headache severities reported in patient's journals
Pain relief at 30, 60, and 240 minutes post-treatment based on headache severities reported in patient's journals
+4 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: Topical, intra-oral ketoprofen gelActive Control1 Intervention
Group II: Placebo gelPlacebo Group1 Intervention
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Who is running the clinical trial?
Behar, Caren, M.D.Lead Sponsor
1 Previous Clinical Trials
67 Total Patients Enrolled
1 Trials studying Migraine
67 Patients Enrolled for Migraine
Caren Behar, MDPrincipal InvestigatorNew York Medical College
1 Previous Clinical Trials
67 Total Patients Enrolled
1 Trials studying Migraine
67 Patients Enrolled for Migraine
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