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Nonsteroidal Anti-inflammatory Drug
Nurtec (Rimegepant) Group for Pain
Phase 4
Waitlist Available
Led By Sergey Motov, MD
Research Sponsored by Antonios Likourezos
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 60 minutes
Awards & highlights
Study Summary
This trial is studying whether using a standardized medication protocol for treating people with migraines in the emergency room results in better patient outcomes than the current standard of care, which can vary depending on the physician, institution, and patient preferences.
Eligible Conditions
- Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 60 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~60 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Pain Score at 60 Minutes
Trial Design
2Treatment groups
Active Control
Group I: Nurtec (Rimegepant) GroupActive Control1 Intervention
Drug: 75 mg of ODT
Group II: AOK GroupActive Control1 Intervention
Drug: Proprietary oral formulation of 0.85mg/kg of ketamine + 324mg of aspirin
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Who is running the clinical trial?
Antonios LikourezosLead Sponsor
38 Previous Clinical Trials
8,573 Total Patients Enrolled
17 Trials studying Pain
1,420 Patients Enrolled for Pain
Sergey Motov, MDPrincipal InvestigatorMaimonides Medical Center
16 Previous Clinical Trials
1,510 Total Patients Enrolled
10 Trials studying Pain
940 Patients Enrolled for Pain
Leily Naraghi, MDPrincipal InvestigatorMaimonides Medical Center
1 Previous Clinical Trials
1 Trials studying Pain
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