Autosomal recessive polycystic kidney disease
MONDO:0009889An inherited disorder characterized by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involvement.
Also known as: AR-PKD, ARPKD, autosomal recessive polycystic kidney, polycystic kidney disease, autosomal recessive, polycystic kidney disease, infantile type, polycystic kidney and hepatic disease 1, polycystic kidney disease, infantile, type I, PKHD1
17 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
-
Sweat sensor could replace needles for kidney patients
Diagnosis CompletedThis study tested a new wearable patch that collects sweat to measure sodium and creatinine levels, which are important for monitoring kidney health and dehydration. Five adults with kidney disease wore the patch while their sweat was analyzed using a special light-based techniqu…
Phase: NA • Sponsor: Korea University • Aim: Diagnosis
Last updated Jun 27, 2026 08:11 UTC
-
New study reveals IVF success for kidney disease carriers
Knowledge-focused CompletedThis study looked at 44 couples where one or both partners have polycystic kidney disease (PKD). They used IVF combined with genetic testing to select embryos without the disease. The goal was to see how often these treatments led to a healthy pregnancy and live birth, and to tra…
Sponsor: Azienda Sanitaria Universitaria Integrata del Trentino • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:08 UTC