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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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2 / Phase 3
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
Placebo
DrugPrimary outcomes
-
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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