Migraine, familial hemiplegic, 2
MONDO:0011232Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.
Also known as: ATP1A2 familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in ATP1A2, migraine, familial hemiplegic, 2, migraine, familial hemiplegic, type 2, FHM2, Mhp2, familial hemiplegic migraine type 2, hemiplegic migraine, familial type 2
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
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ER headache relief: could a steroid combo beat standard painkillers?
Symptom relief Not yet recruitingThis study compares a combination of two drugs (dexamethasone and metoclopramide) against standard painkillers (paracetamol or NSAIDs) for treating severe primary headaches in the emergency department. 94 adults aged 18-60 with a pain score of 5 or higher will be randomly assigne…
Phase: PHASE4 • Sponsor: Pak Emirates Military Hospital • Aim: Symptom relief
Last updated Jun 27, 2026 12:37 UTC
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Teen headache mystery: could uric acid be a clue?
Knowledge-focused Not yet recruitingThis study compares uric acid levels in 80 adolescents (12-18 years) with and without primary headaches. Researchers aim to see if there is a link between uric acid and headaches, which could help understand what causes them. Participants will provide a blood sample and have thei…
Sponsor: Konya Necmettin Erbakan Üniversitesi • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:00 UTC