Lacosamide Versus Propranolol in Migraine

Status Completed

Clinical Trial Summary

Investigators aim to compare the effect of lacosamide versus propranolol in migraine by assessing the absolute reduction in MMD in each group, the percentage of patients who achieved ≥ 50% reduction in the monthly headache days frequency compared to the baseline frequency.

Clinical Trial Description

Investigators will enroll 600 migraine patients who are diagnosed according to ICHD3-beta criteria in our study and will use a questionnaire to detect their demographic and clinical features (disease duration, attack frequency, and duration, pain intensity assessed by the visual analogic scale and we have two groups the first group will include 300 patients and will receive 50 mg lacosamide twice daily, and the second group will receive propranolol 160 mg per day. Investigators will assess The number of migraine days after three months of treatment and the percentage of patients who achieved ≥ 50% reduction in the monthly headache days frequency compared to the baseline frequency (14). HIT-6 score reduction in each group after three months of treatment. The safety of lacosamide was evaluated by monitoring and documenting treatment-emergent adverse events (TEAE) in patients through regular follow-up procedures for three months. ;

Study Design

Related Conditions & MeSH terms

Migraine Disorders

Clinical Trial Details

NCT number	NCT05851781
Study type	Interventional
Source	Kafrelsheikh University
Contact
Status	Completed
Phase	Phase 3
Start date	June 1, 2022
Completion date	August 30, 2023

View Details

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