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Recruiting Phase 2 NCT05867602

NCT05867602 High Dose Albumin in Refractory Ascites

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Clinical Trial Summary
NCT ID NCT05867602
Status Recruiting
Phase Phase 2
Sponsor Baylor College of Medicine
Condition Ascites
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2019-03-25
Primary Completion 2026-03-25

Trial Parameters

Condition Ascites
Sponsor Baylor College of Medicine
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 100
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2019-03-25
Completion 2026-03-25
Interventions
Albumin

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Brief Summary

Advanced cirrhosis with complications is a serious problem imposing a heavy financial burden on health care system. Moreover, ascites is associated with increase in mortality rates among cirrhotic patients. Ascites pathogenesis is multifactorial including: portal hypertension; splanchnic and peripheral arterial vasodilation; and neurohumoral activation. Current management strategies include dietary sodium restriction and diuretic therapy, however, this strategy put patients at the risk of intravascular volume depletion, renal impairment, hepatic encephalopathy and hyponatremia. Moreover, around 10% of patients do not respond to this strategy (termed: diuretics resistant) with 50% of them die within 6 months. This sub-group is managed by frequent large volume paracentesis along with intravenous albumin administration and are usually considered for liver transplantation (LT) and TIPS. Nonetheless, Frequent paracentesis increases the risk of infection, bleeding, bowel perforation, paracentesis-induced circulatory dysfunction (PICD) and renal dysfunction in this sub-group of patients. The beneficial effect of human albumin might result from blood volume expansion tapering activated vasoconstrictor and sodium-retaining systems improving renal perfusion, hence regular infusion of albumin may be beneficial to prevent development of ascites and to improve survival. The positive effects of albumin are supported by previous studies; Romanelli et al, showed a significant increase in survival rate among cirrhotic patients with ascites when compared to those who did not receive albumin. Moreover, a randomized multicenter open label trial published in lancet last year, demonstrated that long term albumin administration improved 18-month survival, decreased the use of paracentesis and decrease in the incidence of cirrhosis related complications among cirrhotic patients with ascites. As of today, there's a limited use of regular high dose albumin in cirrhotic patients with ascites in US, despite being used elsewhere in the world as previously stated. The investigators wish to study long-term efficacy of human albumin administration in patients with decompensated cirrhosis to assess safety and efficacy, and prevention of complications of cirrhosis.

Eligibility Criteria

Inclusion Criteria: 1. Age \> 18 years. 2. patients diagnosed with liver cirrhosis. 3. Refractory ascites which is defined as ascites failing to resolve after maximum tolerable dose of diuretics, and usually require frequent paracentesis. Exclusion Criteria: 1. Patients \< 18y 2. patients with no history of liver cirrhosis 3. patients with refractory ascites but have transjagular intrahepatic portosystemic shunts (TIPS) with previous 3 months 4. Patients with ascites due to other causes, including cardiac, malignant

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