Health Condition 1: G439- Migraine, unspecified
Conditions
Interventions
Intervention1: Amitriptyline: will initially receive amitriptyline 10mg at night for 7 days and then the dose will be increased to 25mg at night for rest of the study.
Intervention2: Propranolol: wil
Sponsors
None
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients presented with migraine according to ICHD 3 criteria 2) NCCT HEAD showing calcified granuloma
Exclusion criteria
Exclusion criteria: 1) Patients who are a k/c/o asthma and ecg s/o AV block or bradycardia. 2)Patients with seizures. 3)Patients refusing consent. 4)Patients already on preventive medications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| We will compare change in headache frequency between the two groups at the end of 1st, 2nd and 3rd months. Timepoint: 1st, 2nd and 3rd months. | — |
Secondary
| Measure | Time frame |
|---|---|
| We will also compare severity of headache [VAS ] and disability caused by headache [ HIT6] between the two groups at the end of 1st, 2nd and 3rd months. Timepoint: 1st, 2nd and 3rd months | — |
Countries
India
Contacts
Public ContactDr Ravi Uniyal
KGMU
Outcome results
None listed