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Clinical Trials/CTRI/2026/02/104411
CTRI/2026/02/104411Not yet recruitingNot Applicable

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

Not applicable1 site in 1 country100 target enrollmentStarted: March 19, 2026Last updated:
Conditions
Drugs

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

Sponsor
Not applicable
Sponsor Class
Other []
Responsible Party
Principal Investigator
Principal Investigator

Dr ASHWIN PAUL

JSS MEDICAL COLLEGE HOSPITAL

Study Sites (1)

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