This Pilot study will enable development \& assessment of a Polycystic Liver Disease-specific patient reported outcomes questionnaire (PLD-Q). Polycystic liver disease (PLD) is characterized by the formation of numerous cysts in the liver, and can lead to severe symptomatic hepatomegaly. It is common in patients with autosomal dominant polycystic liver disease (ADPLD) and autosomal dominant polycystic kidney disease (ADPKD).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Polycystic Liver Disease-specific patient reported outcomes questionnaire (PLD-Q) total score
Timeframe: baseline to 6 months