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临床试验/NCT07354126
NCT07354126招募中不适用

Comparative Efficacy of Flunarizine and Propanolol in Pediatric Migraine Using the PedMIDAS Measuring Tool.

Muhammad Aamir Latif0 个研究点目标入组 44 人开始时间: 2025年9月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
44

研究概览

简要总结

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.

详细描述

Despite the clinical use of flunarizine and propranolol, direct comparisons between these two drugs in children are scarce. This study aims to bridge that gap by evaluating their relative effectiveness and safety as prophylactic treatments for pediatric migraine, addressing a critical unmet need in current research. Considering the routine use of both drugs in clinical practice, the findings would help clinicians to choose the more convenient drug between flunarizine and propranolol as preventive therapy for migraine in their local settings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
8 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 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
  • With a PedMIDAS score ≥11 (moderate-to-severe impact)

排除标准

  • 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
  • Participation in another clinical trial within the last 3 months

研究者

发起方
Muhammad Aamir Latif
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Muhammad Aamir Latif

Research Consultant

RESnTEC, Institute of Research

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