Skip to content

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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06503848
Acronym
MAMBO
Enrollment
108
Registered
2024-07-16
Start date
2024-01-25
Completion date
2024-12-31
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine Disorders

Keywords

migraine, triptan

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.

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.

Interventions

DRUGSumatriptan

Register the response to treatment and headache characteristics.

Sponsors

Instituto de Salud Carlos III
CollaboratorOTHER_GOV
Hospital Universitari Vall d'Hebron Research Institute
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Response to sumatriptan24 hoursRelief of pain from moderate-severe to mild or absent at 2 hours and 24 hours in 3 out of 4 migraine attacks. The response will be evaluated via questionnaire.

Secondary

MeasureTime frameDescription
Migraine characteristics24 hoursPatients will complete a questionnaire describing the characteristics of migraine attacks in the beginning of the attack, and at timepoints 2 and 24 hours after taking sumatriptan.

Countries

Spain

Contacts

Primary ContactMarta Torres-Ferrús, PhD
cefalea@vhir.org(+34)934893000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026