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OpenTrials
Completed

NCT Number: NCT02119052

Effects of Somatostatin on Liver in ADPKD

Autosomal dominant polycystic kidney disease (ADPKD) is associated with the development of a variety of extrarenal manifestations of which polycystic liver disease is most common. The investigators aimed to assess the changes over time of liver volume in ADPKD patients and whether it is affected by the treatment with the somatostatin analogue, octreotide.

35 ADPKD patients (14 males) aged 34±8 years were randomly assigned to 36 month treatment with placebo (n=18) or octreotide (n=17). Clinical and liver parameters at magnetic resonance (RM) were evaluated at baseline, study end and after 24 months of drug withdrawal.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of autosomal dominant polycystic kidney and liver disease
  • glomerular filtration rate greater than 40 ml/min

Exclusion criteria

  • diabetes mellitus
  • proteinuria greater than 1 g/24 hours
  • significant glomerular disease
  • urinary tract lithiasis and infections
  • symptomatic gallstones
  • biliary sludge
  • cancer
  • pregnant women
  • lactanting women

Treatment and study plan

octeotride

Drug

Placebo

Drug

Primary outcomes

  1. Effect of somatostatin on liver volume

    Time frame: 3 years

Sponsors and collaborators

Lead sponsor

Federico II University

Other

Registry information

Official study title

Effect of Long-acting Somatostatin on Liver in Autosomal Dominant Polycystic Kidney Disease

Important dates

Study start
2009
Primary completion
2013
First posted
Apr 21, 2014
Registry last updated
Apr 21, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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