CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 199 enrolled
Drug / intervention
albumin +2 moredrug
Likely dose
albumin 40 gfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00839358
NCT00839358Phase 4Completed

Midodrine and Albumin for Cirrhotic Patients in the Waiting List for Liver Transplantation

Hospital Clinic of Barcelona·interventional·Posted Feb 9, 2009·Updated Aug 18, 2016

In Brief

A Phase 4 clinical trial evaluating albumin, Midodrine, and 1 other intervention for Renal Failure and 4 related conditions. Completed, enrolled 199 participants across 1 site.

Detailed Summary

The aim of this study is to evaluate the effect of prolonged administration of albumin and midodrine on the prevention of complications (renal failure, sepsis, hemorrhage, hepatic encephalopathy and hyponatremia) in patients with cirrhosis in the waiting list for liver transplantation. One hundred and ninety four patients with cirrhosis and awaiting a liver transplantation will include in the study. Patients will be randomized to receive albumin and midodrine (treatment group) or administration of placebo (saline for albumine) and tablets with excipients without midodrine (control group). Patients will be followed-up during 12th months. In the treatment group albumin will be given at a dose of 40g every 15 days and midodrine 5mg tid, in addition with lactitol (conventional doses) and the specific treatment that patients require by cirrhosis. The group control will receive placebo in the same way than the treatment group in addition with lactitol and the specific treatment that they require by their disease. In all the patients liver and renal function test, hormones determination (renin, aldosterone, noradrenaline), and cytokines will be determined in basal conditions. All these determinations will be repeated at month 1st,3rd, 6th and 12th months. Before the inclusion in the study neuropsychological test and critical flicker test will be performed to diagnose minimum EH. These tests will be repeated at 3rd, 6th and 12th months. All the determinations will be repeated at any time that the patients develop any complication considered as an end point. In baseline conditions and at 3rd and 6th months a questionnaire of quality of life (SF36) will be performed. During a year of follow-up the number of paracentesis that patients require, the incidence of renal failure and EH and their relationship with hormonal activity and cytokine levels, free transplant survival and quality of life will be recorded.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain

Timeline

Phase 4CompletedFinished
2009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 9, 2009
Enrollment StartAug 1, 2008
Primary CompletionFeb 1, 2016
TodayJul 2, 2026
Enrollment to primary: 7.5 yearsPosted 17.4 years ago

Interventions

albumindrug

albumine 40 g every 15 days

Midodrinedrug

Midodrine 5mg/8 hs, can be increase up to 8mg/8hs if there is a lack of increase in at least 10mmHg in mean arterial pressure after 15 days of treatment.

Placebodrug

saline solution