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Clinical Trial Summary

This is a multicentre, open, randomised, and controlled trial conducted in sixty (60) patients diagnosed with refractory or recurrent ascites. Patients will be randomised (enrolled) to either treatment arm A- implanted with the ALFApump System or treatment arm B-standard of care with evacuation large volume paracentesis. The main aims of the study are to determine the paracentesis free survival, defined as the time to the first large volume therapeutic paracentesis > 5 litres. The secondary aims are to assess non-inferiority of cirrhosis-related complications in the group of patients randomized to the ALFApump system group, as well as nutritional effects, resource utilisation, patient quality of life and survival non-inferiority.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01528410
Study type Interventional
Source Sequana Medical AG
Contact
Status Completed
Phase Phase 3
Start date August 17, 2012
Completion date September 21, 2016