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RECRUITING
NCT06796725
NA

Prospective Exploratory Study on rTMS for Migraine Under the Guidance of MEG

Sponsor: Ruijin Hospital

View on ClinicalTrials.gov

Summary

Using magnetoencephalography to locate and regulate targets in migraine patients, repeating transcranial magnetic stimulation to physically regulate targets, and evaluating the safety and effectiveness of this treatment method through headache related scales. Using whole genome data and scale scores for correlation analysis, and conducting randomized controls with traditional drugs to explore new approaches for migraine.

Key Details

Gender

All

Age Range

15 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-02-06

Completion Date

2026-06-30

Last Updated

2025-02-11

Healthy Volunteers

No

Interventions

DEVICE

rTMS

(1) The patient undergoes pseudo stimulus intervention in the first week and real stimulus intervention afterwards, which is blind to the patient. (2) Starting from the second week, true stimulation intervention will be conducted for 4 weeks, with each patient making an appointment for 1 month. On Day 7 after the patient intervention, Day 14, Day 30, Day 60, Day 90, Day 180 scales were used to evaluate follow-up.

DRUG

Sibelium

Sibelium 10mg is taken orally every night for 4 weeks each course of treatment. Patients were evaluated and followed up with a scale based on medication intervention, including Day 7, Day 14, Day 30, Day 60, Day 90, and Day 180

Locations (1)

Ruijin Hospital

Shanghai, China