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To compare safety and efficacy of propranolol with flunarizine in adult patients suffering from migraine as prophylactic drugs.

Not Applicable
Conditions
Health Condition 1: G438- Other migraine
Registration Number
CTRI/2023/06/053593
Lead Sponsor
Dr. Rajendra Prasad Government Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Patients willing to give consent.

2) Male and female outpatients between 18-65 years of age with documented history of

migraine (with or without aura) acc. to HIS criteria.

3) Duration of at least 3 months.

4) Frequency of two or more migraine headache per month.

5) Currently not on any prophylactic medication in the last 1 month.

6) Patientsâ?? ability to fill a reliable headache diary successfully.

Exclusion Criteria

1) Patients refusing to give consent.

2) <18 or >65 of age with non-migrainous headache.

3) Pregnant and Lactating women.

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4) Patients with h/o asthma, diabetes, renal, cardiovascular, liver, neoplastic disease,

neurological and mental disorders are excluded.

5) Active alcohol users.

6) Patients allergic or with known contraindications to any of study drugs.

7) Patients who have already taken either of the above-mentioned migraine prophylactic

drugs.

8) Previous unresponsiveness to more than two antimigraine prophylactic drugs.

9) NCCT Head suggesting of any other disease except migraine i.e., abnormal fundus etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
reduction in frequency intensity and severity of migraine attacksTimepoint: at baseline at 4 weeks and at 8 weeks from date of enrollment
Secondary Outcome Measures
NameTimeMethod
to evaluate safety profile to both drugsTimepoint: at baseline at 4 weeks and at 8 weeks from date of enrollment
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