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Autosomal dominant polycystic liver disease
MONDO:0000447An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver.
Also known as: AD polycystic liver disease, ADPLD, PCLD, isolated congenital polycystic liver disease, isolated polycystic liver disease, polycystic liver disease, congenital cystic liver disease, congenital hepatic cyst
3 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Broader categories
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Foam injection may ease pain from polycystic kidney and liver cysts
Symptom relief Recruiting nowThis study looks at whether foam sclerotherapy can reduce pain and improve quality of life for people with autosomal dominant polycystic kidney or liver disease who have large, painful cysts. Researchers will treat 100 adults with 1-3 dominant cysts and follow them for 12 months.…
Sponsor: Mayo Clinic • Aim: Symptom relief
Last updated Jun 27, 2026 08:14 UTC
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New UK registry aims to unlock secrets of polycystic liver disease
Knowledge-focused Recruiting nowThis observational registry is recruiting 500 people with polycystic liver disease (PLD) across the UK. Researchers will collect data from medical records and questionnaires to map how the disease progresses, including symptoms, liver cyst changes, and quality of life. The goal i…
Sponsor: Portsmouth Hospitals NHS Trust • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:05 UTC