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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04511507
Other study ID # Cyto-ALF
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 10, 2016
Est. completion date August 30, 2021

Study information

Verified date September 2021
Source Institutul Clinic Fundeni
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hemoadsorption has been demonstrated to improve liver functional tests in patients with liver failure. The present study investigates the effects of three consecutive sessions of hemoadsorption, performed in accordance to the local protocol for treating patients with acute liver failure, on liver functional tests, severity scores and 30-days mortality. Paraclinical results and severity scores were obtained before and after the three consecutive sessions.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date August 30, 2021
Est. primary completion date August 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients with acute liver failure or acute on chronic liver failure who require hemoadsorption in accordance with local guidelines Exclusion Criteria: - unsigned informed consent - duration of therapy under 12 hours - death before the three consecutive sessions

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
hemoadsorption
three consecutive sessions of hemoadsorption in patients with liver failure

Locations

Country Name City State
Romania Fundeni Clinical Institute Bucharest

Sponsors (1)

Lead Sponsor Collaborator
Institutul Clinic Fundeni

Country where clinical trial is conducted

Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30 days mortality 30 days mortality 30 days
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