Clinical Trial

Laser Acupuncture for Chronic Migraine

Study acronym: LAFCM
Recruiting
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Summary
A single-blind randomized controlled trial was conducted from October 2024 to May 2025. Chronic migraine patients were randomly assigned in a 1:1 ratio to receive either Laser acupuncture or sham treatment. The co-primary outcomes were changes in monthly migraine days (MMD) and acute headache medications usage days per month from baseline, and Hospital Anxiety and Depression Scale (HADS), and Beck's Depression Inventory(BDI) evaluation. Evaluations were taken at baseline and each follow-up point. After \>6 months follow up as washing out time, the sham group received complementary laser acupuncture treatment and follow up for another 3 months, compared the Headache related parameters (onset, duration, pain scale, current medication for headache, menstrual cycle).
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2024-01-12; most recent amendment 2025-11-17.
Status change: Completed → Recruiting 2024-09-13
Trial Details
NCT Number NCT06219694
Lead Sponsor Taichung Veterans General Hospital
Conditions Chronic Migraine
Enrollment 60 participants
Start Date 2022-01-01
Primary Completion 2022-05-04 (estimated)
Study Completion 2025-12-01 (estimated)
Updated on ClinicalTrials.gov 2025-11-20