The aim of this study is to determine the effect of Lanreotide on polycystic liver and kidneys in patients with autosomal dominant polycystic kidney disease.
The aim of this single center observational study is to assess the effect of lanreotide on polycystic liver and kidney. This is achieved by assessing total liver and kidney volume, and several urinary markers that could predict kidney damage or kidney dysfunction, such as GFR, blood pressure, and urinary tubular damage markers and serum biomarker FGF23. The investigators aim to include 43 patients affected by a polycystic liver due to ADPKD. The duration of the trial will be 28 weeks. The treatment will be 24 weeks and the first screening visit will take place four weeks before start of treatment. Eligible patients will be invited to participate.
Study Type
OBSERVATIONAL
Enrollment
43
120 mg every 28 days intramuscular
Radboud University Hospital
Nijmegen, Gelderland, Netherlands
Liver volume
Change in total liver volume between baseline and 24 weeks, as determined by CT volumetry
Time frame: 24 weeks
Kidney volume
Change in kidney volume between baseline and 24 weeks, as determined by CT volumetry
Time frame: 24 weeks
Glomerular filtration rate
Change in GFR between baseline and 24 weeks, as determined by serum and 24 hrs urinary creatinine measurement
Time frame: 24 weeks
Urinary tubular damage markers
Change in urinary tubular damage markers between baseline and 24 weeks
Time frame: 24 weeks
Symptoms
Change in symptoms between baseline and 24 weeks, assessed by GI-questionnaire
Time frame: 24 weeks
Blood pressure
Change in blood pressure between baseline and 24 weeks
Time frame: 24 weeks
quality of life
Change in quality of life between baseline and 24 weeks, measured by EuroQoL-questionnaire
Time frame: 24 weeks
Adverse events
All adverse events that occur during 24 weeks of treatment
Time frame: 24 weeks
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