Randomized control trial on the effects of rifaximin and midodrine combined with standard diuretic therapy versus midodrine with standard diuretic therapy in chronic liver disease patients with refractory ascites
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- To Access whether adding
Study Overview
Brief Summary
Refractory ascites is a serious complication of advanced liver cirrhosis in which ascites does not respond to sodium restriction and standard diuretic therapy or recurs rapidly after therapeutic paracentesis. It is associated with poor prognosis and high mortality. A proportion of patients with cirrhosis and ascites eventually develop refractory ascites, and mortality in this group remains high within one to two years.
Liver transplantation is the only definitive treatment for refractory ascites but is not feasible for many patients due to limited availability and medical or socioeconomic constraints. As a result most patients are managed with diuretics and repeated large volume paracentesis. Diuretic therapy in these patients often leads to complications such as hyponatremia acute kidney injury and hepatic encephalopathy. Recurrent paracentesis increases the risk of infections including spontaneous bacterial peritonitis.
Midodrine improves renal perfusion and renal function by increasing systemic vascular resistance. Rifaximin reduces oxidative stress and splanchnic vasodilation and may improve circulatory dysfunction in cirrhosis. Previous studies have suggested that adding midodrine and rifaximin to standard therapy can enhance diuresis improve renal and systemic hemodynamics and increase short term survival in patients with refractory ascites.
However there is limited data from India regarding the combined use of rifaximin and midodrine in refractory ascites. This study is designed to evaluate whether the addition of rifaximin and midodrine to standard therapy improves diuresis and survival outcomes in patients with refractory ascites.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients diagnosed with Chronic liver disease with refractory ascites.
- •Patients above the age of 18 years.
- •Patients of both gender Informed consent from the patient/ a legally authorised representative.
Exclusion Criteria
- •noncirrhotic causes of ascites primary renal medical diseases, any grade of unresolved hepatic encephalopathy until it has improved and stabilized active gastrointestinal bleeding, Hepato-renal syndrome, previous antibiotic prophylaxis for spontaneous bacterial peritonitis, the presence of hepatocellular carcinoma and portal vein thrombosis active cardiovascular disease, systemic hypertension drugs that affect systemic and renal hemodynamic active alcohol consumption.
Outcomes
Primary Outcomes
To Access whether adding
Time Frame: 12 WEEKS
Rifaximin and midodrine to
Time Frame: 12 WEEKS
standard diuretic therapy
Time Frame: 12 WEEKS
Enhances diuresis and control of
Time Frame: 12 WEEKS
ascites with subsequent weight
Time Frame: 12 WEEKS
loss in patients with refractory
Time Frame: 12 WEEKS
ascites
Time Frame: 12 WEEKS
Secondary Outcomes
- To access the improvement in(renal function and development)
Investigators
Dr ASHWIN PAUL
JSS MEDICAL COLLEGE HOSPITAL
