Migraine, familial hemiplegic, 3
MONDO:0012320Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the SCN1A gene.
Also known as: SCN1A familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in SCN1A, migraine, familial hemiplegic, 3, migraine, familial hemiplegic, type 3, FHM3
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
Migraine drug AJOVY under Real-World safety spotlight
Symptom relief Recruiting nowThis study tracks about 1,000 people with migraine who are taking AJOVY (fremanezumab) as part of their regular care. The goal is to see how safe the drug is over the long term, especially regarding heart problems. Researchers will also collect information on how well it works. T…
Sponsor: Otsuka Pharmaceutical Co., Ltd. • Aim: Symptom relief
Last updated Jun 27, 2026 14:01 UTC
-
Ear needle zaps headaches? new study uses heat cameras to find out
Symptom relief Recruiting nowThis study tests whether inserting a tiny needle into the ear and applying a mild electrical current (called percutaneous needle electrolysis) can help people with frequent headaches. Researchers will use an infrared camera to measure changes in facial skin temperature, since peo…
Phase: NA • Sponsor: University of Alcala • Aim: Symptom relief
Last updated Jun 27, 2026 12:28 UTC
-
The eyes as a window to the brain: can a simple scan monitor MS, Alzheimer's, and Parkinson's?
Knowledge-focused Recruiting nowThis study is testing whether a non-invasive eye scan called optical coherence tomography (OCT) can help track neurological diseases like multiple sclerosis, Alzheimer's, Parkinson's, and migraine. Over two years, researchers will measure the thickness of retinal layers in 840 pa…
Sponsor: IRCCS San Raffaele • Aim: Knowledge-focused
Last updated Jul 24, 2026 00:00 UTC