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临床试验/NCT07103031
NCT07103031已完成不适用

Targeting The Right Pediatric Migraine Patient: A Comorbidity-Oriented Approach To Propranolol Prophylaxis

Kayseri University1 个研究点 分布在 1 个国家目标入组 488 人开始时间: 2021年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
488
试验地点
1
主要终点
Pediatric Migraine Disability Assessment Scale (PedMIDAS) Score

研究概览

简要总结

This observational retrospective cohort study aims to identify clinical and biochemical predictors of response to propranolol prophylaxis in pediatric migraine. A total of 178 children diagnosed with migraine between 2021 and 2023 were evaluated based on headache-related disability (PedMIDAS) and pain severity (VAS). Patients were treated either with behavioral therapy or propranolol (1-3 mg/kg/day) for 3 months.

详细描述

Migraine is a common and disabling neurological condition in the pediatric population, often requiring prophylactic treatment to reduce attack frequency and improve quality of life. Propranolol is frequently prescribed for pediatric migraine prevention; however, treatment response varies considerably among individuals. Understanding the clinical and biochemical factors that predict treatment efficacy could enhance individualized care and reduce unnecessary medication use.

This retrospective cohort study evaluated 178 children diagnosed with pediatric migraine between January 2021 and December 2023 at a tertiary neurology outpatient clinic. All participants were assessed using the Pediatric Migraine Disability Assessment Scale (PedMIDAS) and Visual Analog Scale (VAS) before and after treatment. Patients received either behavioral therapy or oral propranolol (1-3 mg/kg/day) for a duration of 3 months, based on clinical indication and family preference.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
2 Years 至 19 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children aged 0-20 years
  • Diagnosed with primary headache according to the International Classification of Headache Disorders, 3rd edition (ICHD-3)
  • Clinical and/or neurological evaluation consistent with primary headache
  • Completed baseline PedMIDAS and VAS assessments
  • Available for 3-month follow-up after initiation of treatment

排除标准

  • Diagnosis of secondary headache, based on clinical history, family history, neurological examination, or laboratory/imaging findings
  • Failure to meet ICHD-3 diagnostic criteria for primary headache
  • Presence of structural brain lesions or other neurological disorders
  • Chronic systemic illness or current use of other migraine prophylactic medications
  • Incomplete data or loss to follow-up within the 3-month period

研究组 & 干预措施

Group 1

Behavioral therapy group

干预措施: Behavioral therapy (Behavioral)

Group 2

Propranolol group

干预措施: Propranolol (Drug)

结局指标

主要结局

Pediatric Migraine Disability Assessment Scale (PedMIDAS) Score

时间窗: Baseline to 3 months after treatment

The primary outcome is the change in PedMIDAS score from baseline to 3 months after treatment. PedMIDAS is a validated questionnaire that quantifies migraine-related disability in children and adolescents. A greater reduction indicates improved clinical response.

次要结局

  • Visual Analog Scale (VAS) Pain Scores(Baseline to 3 months after treatment)

研究者

发起方
Kayseri University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Özge BAYKAN ÇOPUROĞLU

Asst. Prof.

Kayseri University

研究点 (1)

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