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Clinical Trial Summary

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.


Clinical Trial Description

The study consists of an initial visit coinciding with the start of treatment, a subsequent visit after 6 months of treatment and finally another after 12 months, coinciding with the end of treatment. In case of worsening after suspension, a clinical visit will be carried out at the time of worsening to evaluate the reintroduction of the drug and in case of reintroduction, a visit will be carried out after 3 months. If patients do not worsen, a visit will be made 6 months after completing treatment. At each visit, demographic and clinical variables will be collected. In addition, 3 blood tests will be performed corresponding to the beginning of treatment, after 6 months and a month and a half from the last infiltration. Likewise, a brain MRI will be obtained prior to the start of treatment. These blood samples and neuroimaging data will be processed for subsequent analysis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06459648
Study type Observational [Patient Registry]
Source Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
Contact Ana Beatriz Gago Veiga
Phone +34 915202416
Email anabeatriz.gago@salud.madrid.org
Status Recruiting
Phase
Start date April 26, 2023
Completion date December 2025

See also
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