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Single Pass Albumin Dialysis in Patients With Cirrhosis

Prospective Pilot Study Assessing Safety and Efficacy of Single Pass Albumin Dialysis in Patients With Acute on Chronic Liver Failure

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00764049
Acronym
DACAR
Enrollment
11
Registered
2008-10-01
Start date
2009-06-30
Completion date
2012-07-31
Last updated
2015-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute on Chronic Hepatic Failure, Cirrhosis, Encephalopathy, Hepatorenal Syndrome

Keywords

Albumin dialysis, Artificial liver support, Acute on chronic liver failure

Brief summary

The aim of this study is to determine whether a simplified device of albumin dialysis also has beneficial effects.

Detailed description

Albumin dialysis has beneficial effects in patients with acute on chronic liver failure. However, current devices are complex and costly. The aim of this study is to determine whether a simplified device of albumin dialysis also has beneficial effects.

Interventions

DEVICESingle pass albumin dialysis

6 hours sessions of albumin dialysis.

Sponsors

Laboratoire français de Fractionnement et de Biotechnologies
CollaboratorINDUSTRY
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Minimum age of 18 years * Written consent after information of the patient or, in case of inability, by a parent or a close if he is present. * Patient having a cirrhosis researched by previous exams (liver biopsy) or, in the absence of previous diagnosis, diagnosed in view of the results of clinical, biological and morphological data, whatever the origin of the cirrhosis (virus of hepatitis B, virus of hepatitis C, extreme consumption of alcohol or other reasons)

Exclusion criteria

* Participation to an other study in the 4 weeks before * Active digestive bleeding, unchecked by the pharmacological treatments and the endoscopic techniques.

Design outcomes

Primary

MeasureTime frame
Effects on clinical and biochemical variables3 months follow-up

Secondary

MeasureTime frame
Safety3 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026