Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT06459648

Study for Prevent Chronification Migraine Through Prediction of Response to Treatment With Anti-CGRP Antibodies

Led by Fundación de Investigación Biomédica - Hospital Universitario de La Princesa · Updated on 2025-09-24

350

Participants Needed

7

Research Sites

135 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Being able to predict each patients response to a specific treatment can mean a significant improvement in socioeconomic costs, but above all in their quality of life. With the present study, the investigators aim to analyze in a combined way different clinical, biological and neuroimaging variables, which allow the clinical staff to anticipate the response to treatment with anti-CGRP monoclonal antibodies in patients with migraine.

CONDITIONS

Official Title

Study for Prevent Chronification Migraine Through Prediction of Response to Treatment With Anti-CGRP Antibodies

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged between 18 and 65 years.
  • Caucasian ethnicity.
  • Diagnosed with migraine with or without high-frequency episodic aura (more than 8 days of migraine per month) or chronic migraine by a headache expert using International Classification of Headache Diseases, 3rd edition criteria.
  • History of migraine for at least one year.
  • Stable preventive treatment for at least one month before starting monoclonal antibody treatment and no botulinum toxin in the month prior.
  • Able to describe their clinical situation and headache characteristics.
  • Provide informed consent.
Not Eligible

You will not qualify if you...

  • Any other type of headache besides migraine, except for headache caused by overuse of pain medication.
  • Presence of neurological abnormalities on examination.
  • Pregnancy or breastfeeding.
  • Cognitive impairment or conditions that prevent proper study participation.
  • Need for changes in preventive treatment during the first 6 months after starting monoclonal antibody treatment.
  • Significant adverse effects requiring stopping or changing anti-CGRP treatment.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

Hospital Clínico Universitario Lozano Blesa

Zaragoza, Aragon, Spain, 50009

Actively Recruiting

2

Hospital Universitario Donostia

Donostia / San Sebastian, Basque Country, Spain, 20014

Actively Recruiting

3

Hospital Universitario Marqués de Valdecilla

Santander, Cantabria, Spain, 39008

Actively Recruiting

4

Hospital Clínico Universitario de Valladolid

Valladolid, Castille and León, Spain, 47010

Actively Recruiting

5

Hospital Universitari Vall d'Hebron Research Institute

Barcelona, Catalonia, Spain, 08035

Actively Recruiting

6

Hospital Universitario de La Princesa

Madrid, Madrid, Spain, 28006

Actively Recruiting

7

Hospital Universitario Politécnico La Fe

Valencia, Valencia, Spain, 46026

Actively Recruiting

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Research Team

A

Ana Beatriz Gago Veiga

CONTACT

I

Iris Fernández Lázaro

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

1

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