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r-TMS on post-stroke headaches

Phase 3
Recruiting
Conditions
r-TMS on post-stroke headaches.
Other disorders of blood and blood-forming organs in diseases classified elsewhere
Registration Number
IRCT20181005041236N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
48
Inclusion Criteria

Includes all patients with CVA with headache

Exclusion Criteria

Unrelated patients with CVA? People with headache other than CVA such as migraine and tension headaches, people with malignant diseases
Non-participation in the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Determination of the mean headache after stroke in the study group before and after the procedure rtms. Timepoint: For each patient for 20 minutes for 10 sessions up to 6 months. Method of measurement: Based on the VAS scale for pain.
Secondary Outcome Measures
NameTimeMethod
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