RecruitingNCT05554835
Rare condition
Very long chain acyl-CoA dehydrogenase deficiency
3
studies recruiting now
as of 7 Sept 2026
26
studies registered in total
as of 7 Sept 2026
5
countries with a recruiting site
as of 7 Sept 2026
30 Aug 2023
most recent study posted
among recruiting studies
Recruiting trials
RecruitingPhase 2NCT06017869
Evaluate the Safety and Therapeutic Effects of a Single Intravenous Infusion (IV) of Autologous CD34+ Cells Enriched With Allogenic Placenta-derived Mitochondria in Patients With a Diagnosis of Pearson Syndrome (PS)
RecruitingNCT04602325
Systemic Biomarkers of Brain Injury From Hyperammonemia
Showing the 3 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
Search all Very long chain acyl-CoA dehydrogenase deficiency studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Very long chain acyl-CoA dehydrogenase deficiency
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (ACADVL).
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).