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Polycystic Liver Disease Registry (UK)

Polycystic Liver Disease Registry (UK)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04645251
Acronym
PLD
Enrollment
500
Registered
2020-11-27
Start date
2021-01-21
Completion date
2030-12-01
Last updated
2025-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Liver Disease

Brief summary

Multicentre, observational registry studying the natural course of polycystic liver disease.

Detailed description

The Polycystic Liver Disease (PLD) registry (UK) is the UK specific part of an international, multicentre, observational registry. The overall international PLD registry is led by Radboud University Medical Center, Nijmegan, Netherlands. Note- please direct any queries about the international registry to the team at Radboud University Medical Center. All patients with Polycystic Kidney Disease (PKD) with PLD or patients with Isolated (without PKD) Polycystic Liver Disease are eligible for inclusion (\>10 liver cysts). Data will be collected prospectively and retrospectively including a specific validated PLD questionnaire (PLD-Q). This registry provides us insight in patient characteristics, risk factors, symptoms, quality of life and treatment strategies in the biggest international PLD cohort so far. Results of this registry will be published and shared at national and international congresses.

Interventions

None listed

Sponsors

Radboud University Medical Center
CollaboratorOTHER
Portsmouth Hospitals NHS Trust
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with PLD with more than 10 liver cysts * Patients with PKD and PLD with more than 10 liver cysts

Exclusion criteria

* Patients with PKD or PLD with less than 10 liver cysts

Design outcomes

Primary

MeasureTime frameDescription
Map the natural course of PLD10 yearsTo establish the demographics, presence and severity of symptoms (quantified using the validated PLD-Q questionnaire), liver cyst characteristics on imaging (assessed using Qian's classification), biochemical marker abnormalities (including gamma-glutamyl transferase and alkaline phosphatase), rate and nature of complications, need for treatment, change in liver volume in patients with PLD. This data will be collected retrospectively and prospectively from clinical records and the PLD-Q questionnaire.

Secondary

MeasureTime frameDescription
Assess quality of life using the validated PLD questionnaire (PLD-Q)10 yearsThe PLD-Q questionnaire consists of 18 items assessing symptom frequency and severity. It gives a score (0-100) based on the patient's answers with a higher score indicating more severe, symptomatic disease with a poorer quality of life.
Elucidate risk factors for developing a complication in PLD10 yearsFor patients that develop a complication of PLD (including jaundice, abdominal hernia, features of portal hypertension, cyst haemorrhage and cyst infection) we will look through their clinical record to establish if there any risk factors which are common to those with a complication (e.g. age, gender, medications, cyst phenotype).
Elucidate elements that affect PLD progression10 yearsFor patients that have a worsening of their PLD (based on increasing symptoms as per the PLD-Q questionnaire, development of complications or need for treatment) we will look through their clinical records to establish if there any elements which are common to those with progressive disease (e.g. age, gender, medications).
Compare effectiveness of different therapies10 yearsFor patients who have had or require treatment for PLD we will compare the effectiveness of that treatment based on change in symptoms (based on PLD-Q questionnaire), recurrence of symptoms, development of complications or need for further treatment.
Determine whether rate of liver growth can be used to predict disease progression10 yearsLiver growth rate will be determined using change in liver volume on serial radiology imaging. This will be compared against patients symptoms (measured via PLD-Q questionnaire), development of complications and need for treatment to establish whether there is a correlation in rate of liver growth and disease progression

Countries

Netherlands, United Kingdom

Contacts

Primary ContactRichard Aspinall, BSc, MBChB, PhD
richard.aspinall@porthosp.nhs.uk02392286255
Backup ContactBenjamin Giles, BSc, MBBS
benjamin.giles@porthosp.nhs.uk02392286000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026