Comparative Efficacy of Flunarizine and Propanolol in Pediatric Migraine

ConditionMigraine
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-15
SponsorMuhammad Aamir Latif

About this trial

Flunarizine and propranolol have demonstrated efficacy in reducing migraine frequency across age groups, though evidence in pediatric populations remains limited and inconsistent. Therefore, the current study has been planned to evaluate and compare the effectiveness of flunarizine and propranolol in reducing migraine frequency in children aged 8-15 using the Pediatric Migraine Disability Assessment Scale (PedMIDAS) score.

Eligibility criteria

Qualifiers

Children of any gender

Aged 8-15 years

Diagnosed with migraine (with/without aura) per International Classification of Headache Disorders, 3rd Edition (ICHD-3) criteria

A history of ≥4 migraine attacks/month for the preceding 3 months

Disqualifiers

Children with secondary headache disorders (e.g., due to infections, trauma, structural brain lesions)

Known hypersensitivity or contraindications to flunarizine or propranolol

Presence of cardiovascular disorders (e.g., bradycardia, heart block, hypotension, asthma)

Non-compliance or inability to attend regular follow-ups

Trial design

Treatments tested in this trial

  • Flunarizine
  • Propranolol

Treatment groups

44 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Muhammad Aamir Latif

Lead sponsor

RESnTEC, Institute of Research

Sponsor institution