Actively Recruiting

Age: 18Years - 50Years
All Genders
NCT07177885

Tryptophan as a Modulating Factor in the Antimigraine Efficacy of Triptans

Led by University Hospital, Clermont-Ferrand · Updated on 2026-03-09

144

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Clermont-Ferrand

Lead Sponsor

U

University of the Basque Country (UPV/EHU)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Migraine is a leading cause of disability, and while triptans are commonly used to treat migraine attacks, over 20% of patients don't respond well to them. This study aims to understand why some people don't benefit from triptans. One key focus is tryptophan, an amino acid that plays a role in migraine and is involved in producing serotonin, which affects pain and inflammation. The study will compare levels of tryptophan and its by-products in patients who respond well to triptans versus those who don't. It will also look at how conditions like inflammatory bowel disease may affect tryptophan absorption. The goal is to improve migraine treatments tailored to different patient needs, though participants may not experience immediate personal benefits.

CONDITIONS

Official Title

Tryptophan as a Modulating Factor in the Antimigraine Efficacy of Triptans

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Cisgender women, premenopausal, aged 18 to 50 years
  • Cisgender men, aged 18 to 50 years
  • Diagnosed with migraine (according to ICHD-3 criteria)
  • Diagnosed as responders or non-responders to triptans (according to the criteria of Sacco et al., 2022)
  • Permitted comparison groups include triptans used alone or with other migraine treatments such as NSAIDs, acetaminophen, ergotamine, opioids, or antiemetics
  • All routes of administration and dosages of triptans allowed
  • Affiliated with a social security system
Not Eligible

You will not qualify if you...

  • Patients under guardianship, curatorship, deprivation of liberty, or legal protection
  • Pregnant and breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU de Clermont-Ferrand

Clermont-Ferrand, France

Actively Recruiting

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Research Team

L

Lise Laclautre

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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