Migraine Attack Treatment Response Molecular and Clinical BiOmarkers (MAMBO) Phase I

Last updated: October 24, 2024
Sponsor: Hospital Universitari Vall d'Hebron Research Institute
Overall Status: Active - Recruiting

Phase

N/A

Condition

Migraine (Adult)

Oral Facial Pain

Treatment

Sumatriptan

Clinical Study ID

NCT06503848
EOM(AG)053/2022(6055)
  • Ages 18-45
  • All Genders

Study Summary

The goal of this observational study is to identify differential traits in spontaneous migraine attacks that can help us predict the response to treatment with sumatriptan.

Participants will be asked to register the headache characteristics before and after taking sumatriptan and whether the treatment was effective or not during four migraine attacks.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Migraine with or without aura diagnosis according to ICHD-3 criteria

  • <8 migraine days per month

  • Be able to read, write and understand instructions.

  • Have internet access and mail address

  • Signing of the informed consent

Exclusion

Exclusion Criteria:

  • Active preventive treatment for migraine

  • Active medication with an effect over the central nervous system

  • Serious physical or psychiatric condition

  • Cardiovascular or hepatic disease

  • Pregnant or breastfeeding women

  • Any triptan contraindication

  • Severe migraine attacks without previous response to triptans or NSAIDs

Study Design

Total Participants: 108
Treatment Group(s): 1
Primary Treatment: Sumatriptan
Phase:
Study Start date:
January 25, 2024
Estimated Completion Date:
December 31, 2024

Study Description

There is still an unmet need in acute migraine treatment, some patients don't respond properly to acute medication.

There are some interindividual differences in clinical characteristics of migraine attacks. These differences may determine the response to acute treatment. Describing the phenotypical differences between patients who are responders and patients non-responders will allow us to offer a personalized treatment.

The aim of the study is to determine which characteristics are associated with a response or a non-response to acute treatment with sumatriptan.

Participants will be asked to register the headache characteristics and accompanying symptoms during 4 spontaneous migraine attacks and its response to treatment with sumatriptan.

Connect with a study center

  • Hospital Universitari Vall d'Hebron

    Barcelona,
    Spain

    Active - Recruiting

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