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High versus Low volume plasma exchange in liver failure

Comparative efficacy of standard volume plasma exchange Vs high volume plasma exchange in patients with acute on chronic liver failure- A randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019660
Enrollment
20
Registered
2019-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K729- Hepatic failure, unspecified

Interventions

Intervention1: High Volume plasma exchange: Plasma exchange shall be performed at the bedside on the enrolled patients at liver HDU (Department of Hepatology) on three consecutive days, using a contin

Sponsors

Post Graduate Institute of Medical Education and Research Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. First episode of de-compensation with AARC-ACLF (APASL (Asian Pacific Association for the Study of the Liver) ACLF (Acute on Chronic Liver Failure) Research Consortium (AARC) grade I or II (AARC score 2. No evidence of active infection 3. Willing to give informed consent for the procedure

Exclusion criteria

Exclusion criteria: 1. Pregnancy 2. Co-existing HCC or extra-hepatic malignancy 3. Microbiological or radiological evidence of active infection 4. Active hemorrhage 5. Multi-organ failure(>= 3 organ failures) 6. APASL-AARC score >10 7. Known allergy to Plasma, Protamine or Heparin.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy (in term of change of clinical grade of severity) and tolerability (in terms of adverse events related to procedure) of standard (one) volume plasma exchange Vs high volume plasma exchange in acute on chronic liver failure patientsTimepoint: Day 0, Day 4, day 30 and day 90

Secondary

MeasureTime frame
To estimate the effect of different volume exchange procedure on biochemical parameters and Cytokine levels (IL6 IL10 and TNFα) To compare the effect of different volume exchange procedures on 30 & 90 day mortality. Timepoint: Day 0 to day 4 for biochemical and laboratory parameters and day 30 and day 90 for mortality

Countries

India

Contacts

Public ContactRekha Hans

Post Graduate Institute of Medical Education and Research, Chandigarh

drhansrekha@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026