NCT06221111

Comparison of Rimegepant and Placebo for Pain in IBS

Rimegepant, a CGRP Antagonist, in the Treatment of Visceral Sensation and Chronic Abdominal Pain: A Pilot Study
Mayo Clinic·Phase 4·ClinicalTrials.gov·drugNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Irritable Bowel Syndrome
Drug/Device/Intervention
Rimegepant 75 MG [Nurtec]
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Mayo Clinic
Location
Rochester, United States of America
Timeline & enrollment
Phase
Phase 4
Start date
Apr 15, 2024
End date
Jun 01, 2025
Enrollment
24 participants
Primary outcome

abdominal pain

Summary

The primary aim of this study is to evaluate the efficacy of rimegepant on abdominal pain
 scores in participants with non-constipation IBS.

ICD-10 classifications
Irritable bowel syndromeOther and unspecified irritable bowel syndromeIrritable bowel syndrome with mixed bowel habits [IBS-M]Irritable bowel syndrome with predominant constipation [IBS-C]Irritable bowel syndrome with predominant diarrhoea [IBS-D]
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06221111
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06221111 through Pure Global AI's free database. This Phase 4 trial is sponsored by Mayo Clinic and is currently Not yet recruiting. The study focuses on Irritable Bowel Syndrome. Target enrollment is 24 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.