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NCT06532357Completed

A Study to Learn About the Benefit of Rimegepant Versus Triptans in Migraine Buddy App Users.

Evaluation of Satisfaction With Rimegepant and Triptans Utilizing Migraine Buddy Retrospective Data

Source: ClinicalTrials.gov · Last updated 22 Aug 2025

Brief summary (registry, in English)

The purpose of this study is to collect information of the US users from the Migraine Buddy app between 20 October 2023 and 20 May 2024. Patients who used Nurtec and/or triptans as an acute treatment for migraine, with or without a background of preventive treatment (anti-CGRP, Botox or oral migraine preventive medications) and completed a survey were eligible for this study. Acute treatment is a short-term treatment. The aim of this retrospective analysis was to learn about the user´s satisfaction with Nurtec or the triptan. The level of satisfaction with Nurtec will be compared to the level of satisfaction with triptans. The benefit of this study is the real-life setting of the information collected. This means that the users were using the Migraine Buddy app for tracking their migraines in real life.

Status (registry)
Completed
Study type
Observational
Enrollment
1536 (actual)
First submitted
29 Jul 2024
Start date
9 Jun 2024
Primary completion date
10 Jun 2024
Lead sponsor
Pfizer
Diseases
Migraine
NCT number
NCT06532357

What you commit to

  • Study type: Observational
  • Participants enrolled: 1536
  • From 9 Jun 2024 to the primary completion date, 10 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Users who did not report using either medication for which they complete the survey within 60 days prior to the survey.

Who the study is looking for

  • Patients who used Nurtec and/or triptans as an acute treatment for migraine, with or without a background of preventive treatment (anti-CGRP, Botox or oral migraine preventive medications).
  • Male or female participants with migraine
  • Having consented to the anonymous use of their data for research
  • Currently using Nurtec and/or triptans to treat migraine attacks

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Pfizer
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.