Polycystic Liver Disease Registry (UK)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPortsmouth Hospitals NHS Trust

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients with PLD with more than 10 liver cysts

Patients with PKD and PLD with more than 10 liver cysts

Disqualifiers

Patients with PKD or PLD with less than 10 liver cysts

Trial population

Mixture of adult patients with PKD and PLD

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Map the natural course of PLD

To 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.

Time frame
10 years

Secondary outcomes

1

Assess quality of life using the validated PLD questionnaire (PLD-Q)

The 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.

Time frame
10 years
2

Elucidate risk factors for developing a complication in PLD

For 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).

Time frame
10 years
3

Elucidate elements that affect PLD progression

For 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).

Time frame
10 years
4

Compare effectiveness of different therapies

For 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.

Time frame
10 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Portsmouth Hospitals NHS Trust

Lead sponsor

Radboud University Medical Center

Collaborator