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NCT06503848 | RECRUITING | Migraine Disorders


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

Vall d'Hebron University Hospital Research Institute

Brief 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.

Condition or disease

Migraine Disorders

Intervention/treatment

Sumatriptan

Detailed 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.

Study Type : OBSERVATIONAL
Estimated Enrollment : 108 participants
Official Title : Migraine Attack Treatment Response Molecular and Clinical BiOmarkers (The MAMBO Study) Phase I
Actual Study Start Date : 2024-01-25
Estimated Primary Completion Date : 2024-12
Estimated Study Completion Date : 2024-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years to 45 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
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 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

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

Location Details

NCT06503848


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Locations


RECRUITING

Spain,

Vall d'Hebron University Hospital

Barcelona, Spain,

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