Study to compare the efficacy and impact on quality of life of two types of repetitive transcranial magnetic stimulation in chronic migraine patients
Phase 4
- Conditions
- Health Condition 1: G437- Chronic migraine without aura
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with migraine without aura with duration of symptoms for more than 15 days in a month for 3 months; non-responsive to medical treatment and willing to give consent will be included in the study.
Exclusion Criteria
Patients with headache secondary to Chronic tension-type and medication overuse
Patients with abnormal computed tomography (CT) or magnetic resonance imaging (MRI) of the brain or with abnormal conventional EEG
Patients with depression as determined by Hamilton Depression scale
Patients with secondary causes of Headache
Pregnant females
Patients with epilepsy or family history of epilepsy
Patients with a pacemaker, intracranial metal objects, and artificial metal tooth will be excluded also from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To look for severity of headache reduction between both the groupsTimepoint: 1 and 3 months
- Secondary Outcome Measures
Name Time Method To look for improvement in quality of life after treatment between both the groupsTimepoint: 3 and 6 months