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NCT02719210

High Volume Plasma Exchange in Children With Acute Liver Failure and Acute on Chronic Liver Failure

Completed NA Last updated 6 December 2018
What this trial tests

NA trial testing High Volume Plasma Exchange in Acute Liver Failure in 75 participants. Completed in 30 November 2018.

Timeline
1 January 2016
Primary endpoint
30 November 2018
30 November 2018

Quick facts

Lead sponsorInstitute of Liver and Biliary Sciences, India
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment75
Start date1 January 2016
Primary completion30 November 2018
Estimated completion30 November 2018
Sites1 location across India

Drugs / interventions tested

Conditions studied

Sponsor

Institute of Liver and Biliary Sciences, India

Who can join

Adults 1 to 18, any sex, with Acute Liver Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

All the children with acute liver failure who are candidates for transplant but have constraints for transplant will be randomized either to receive standard medical therapy or high volume plasma exchange along with standard medical therapy with the aim to assess the effect of high volume plasma exchange on transplant free survival.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of High Volume Plasma Exchange

Trials testing the same drug.

Other recruiting trials for Acute Liver Failure

Currently open trials in the same condition.

Other Institute of Liver and Biliary Sciences, India trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02719210.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing