Comorbidity-Based Propranolol Use in Pediatric Migraine

CompletedOBSERVATIONAL
Enrollment

488

Participants

Timeline

Start Date

January 1, 2021

Primary Completion Date

December 31, 2022

Study Completion Date

December 31, 2023

Conditions
Pediatric MigraineMigraine Disorders, BrainVitamin D Deficiency
Interventions
BEHAVIORAL

Behavioral therapy

Patients in PedMIDAS stage 1-2 (score ≤ 30) received behavioral therapy including lifestyle counseling, stress management techniques, sleep hygiene education, and individualized headache triggers review. Additionally, each patient was provided with a headache report card to self-monitor symptoms, triggers, and medication use over a 3-month period.

DRUG

Propranolol

Patients in PedMIDAS stage 3-4 (score \> 30) received oral propranolol treatment at a dose of 1-3 mg/kg/day, adjusted by weight and tolerance, for a total of 3 months. The medication was prescribed and monitored by a pediatric neurologist. Patients were followed with routine check-ups and adverse effects were recorded.

Trial Locations (1)

38130

Kayseri University, Kayseri

All Listed Sponsors
lead

Kayseri University

OTHER

NCT07103031 - Comorbidity-Based Propranolol Use in Pediatric Migraine | Biotech Hunter | Biotech Hunter