drugset / Trial / NCT00359437
Satavaptan in the Prevention of Ascites Recurrence in Patients With Ascites Due to Cirrhosis of the Liver
RandomizedParallel-groupDouble-blindTreatment
Summary
Primary To evaluate the efficacy of satavaptan on top of diuretic drugs in reducing the recurrence of ascites. Secondary To evaluate the tolerability and safety of satavaptan on top of diuretic drugs over a 52-week treatment period in participants with cirrhosis of the liver and recurrent ascites. The one-year double blind placebo controlled period is extended up to 2 years in a long term safety study (PASCCAL-2).
Timeline
- Start
- 2006-07
- Primary completion
- 2008-10
- Completion
- 2008-10
Outcome
Missed primary endpoint
paper Satavaptan was not more effective than placebo in the control of ascites in any of the populations studied as estimated by the primary efficacy endpoints: PMID 21836029 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | satavaptan | Small molecule | 5 mg | Oral |
| Subject | satavaptan | Small molecule | 10 mg | Oral |