Parkinson disease 22, autosomal dominant
MONDO:0014742Any Parkinson disease in which the cause of the disease is a mutation in the CHCHD2 gene.
Also known as: CHCHD2 Parkinson disease, PARK22, Parkinson disease 22, autosomal dominant, Parkinson disease 22, autosomal dominant; PARK22, Parkinson disease caused by mutation in CHCHD2
11 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
Could stem cells ease Parkinson's symptoms? new trial launches
Disease control Not yet recruitingThis study tests two types of stem cell treatments for people with Parkinsonism, a condition that causes movement and non-movement problems. The goal is to see if these treatments are safe and can improve symptoms like tremors, stiffness, and mood changes. About 120 adults aged 4…
Phase: PHASE2 • Sponsor: Biocells Medical • Aim: Disease control
Last updated Jun 27, 2026 11:00 UTC
-
Could zapping the spine steady blood pressure in Parkinson's?
Disease control Not yet recruitingThis study tests whether spinal cord stimulation can help people with Parkinson's disease who experience sudden drops in blood pressure when standing up. Forty participants will receive either an implanted stimulator or a non-invasive version. The goal is to see if the treatment …
Phase: NA • Sponsor: Ruijin Hospital • Aim: Disease control
Last updated Jun 27, 2026 08:09 UTC