Suppressive Functions of Regulatory T Cells in Migraine
- NCT ID
- NCT07067112
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- University Hospital, Clermont-Ferrand
- Conditions
- Chronic Migraine
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 24 participants (Estimated).
What is being studied
- Biological: Blood sampling, questionnaire and phone call
- Intervention: Blood Specimen Collection
- Intervention: Clinical Laboratory Techniques
- Intervention: Data Collection
- Intervention: Diagnosis
- Intervention: Diagnostic Techniques and Procedures
- Intervention: Environment and Public Health
- Intervention: Epidemiologic Methods
- Intervention: Health Care Evaluation Mechanisms
- Intervention: Health Care Quality, Access, and Evaluation
- Intervention: Investigative Techniques
- Intervention: Public Health
- Intervention: Punctures
- Intervention: Quality of Health Care
- Intervention: Specimen Handling
- Intervention: Surgical Procedures, Operative
- Intervention: Surveys and Questionnaires
Who may be eligible
- Ages
- 18 Years to 50 Years
- Sex
- Female
- Healthy volunteers accepted
- Yes
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Females
* 18 to 50 years old
* For chronic migrain : At least 8 monthly migraine days
Exclusion Criteria:
* BMI \< or = 17kg/m² or \> or = 30kg/m²
* Diagnosis or suspicion of type 2 diabetes, auto-immune or inflammatory diseases, immunodeficiency diseases
* Diagnosis of headache of non-migraine origin, except for tension type headache (i.e.: cluster headache, post-traumatic headache, cerebral tumour…)
* For controls participants : tension type headache with 4 or more monthly headache days
* Pregnancy, delivery, miscarriage, breastfeeding, participation in a medically assisted human reproduction program (ovary stimulation/hormone therapy) \< 3 months before blood sampling
* Menopause, hysterectomy, or bilateral oophorectomy
* Modification of prophylactic anti-migraine therapy (start, change of molecule, interruption) \< 1 month before blood sampling (for migraine participants)
* Hormone therapy (beside contraception and treatment of endometriosis)
* Transplantation (solid organ or bone marrow)
* Cancer (active or remitting) \< 1 year before blood sampling (solid organ or blood)
* Haematologic disease (benign or malignant) of the lymphoid lineage
* Guardianship, curatorship, safeguard of justice or deprivation of liberty
* For controls : history of migraine
Study locations
1 study location is listed.
Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.
Countries: France
Sample of listed locations
- CHU Clermont-Ferrand — Clermont-Ferrand, France — Recruiting
Study details
- Start date
- September 10, 2026
- Primary completion date
- November 30, 2027
- Completion date
- November 30, 2027
- First posted
- July 16, 2025
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07067112
- Registry last updated
- October 14, 2026
- QualifiedStudies registry data refreshed
- October 19, 2026
- QualifiedStudies record fetched
- October 19, 2026
View NCT07067112 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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