Clinical Trials Directory

Trials / Completed

CompletedNCT01354405

Somatostatin Analogues as a Volume Reducing Treatment of Polycystic Livers (RESOLVE)

The Effect of Lanreotide on Volume of Polycystic Liver and Kidney in Autosomal Dominant Polycystic Kidney Disease

Status
Completed
Phase
Study type
Observational
Enrollment
43 (actual)
Sponsor
Radboud University Medical Center · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DRUGLanreotide120 mg every 28 days intramuscular

Timeline

Start date
2011-05-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2011-05-16
Last updated
2014-07-09

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01354405. Inclusion in this directory is not an endorsement.