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Exploring the Role of Albumin Therapy in Affecting Post-Surgical Abdominal Drainage in ICU Patients After Liver Transplant

Efficacy of albumin infusion for hypoalbuminemia in post operative period in living donor liver transplantation – An open label randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071234
Enrollment
74
Registered
2024-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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: Human albumin intravenous infusion: Dose: 20gram (20% Albumin)
Frequency: Once/Twice a day
Route of Administration: Intravenous Slow Infusion
Total Duration: For 5 days after the liver transplant surgery Control Intervention1: No human albumin intravenous infusion: None Control Intervention2: Placebo infusion (Normal Saline): Dose: 100-200m
Total Duration: For 5 days after the liver transplant surgery

Sponsors

Dr Subhash Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Immediate post living donor liver transplant recipients (Aged greater than 18 years) admitted to the liver transplant intensive care unit

Exclusion criteria

Exclusion criteria: 1)Pregnancy, 2)Age less than 18 years, 3)Re-transplantation, 4)Deceased donor LT, 5)Greater than 3 organ failure (ACLF grade 3), 6)Pre LT rapid filling ascites or Grade 3 ascites, 7)Primary graft failure, 8)Post LT vascular or biliary complication, 9)Negative consent, 10)Post LT correction of hypoalbuminemia (Sepsis, Hemodynamic instability, acute kidney injury), 11)Graft weight less than 600 grams, 12)Combined liver-kidney transplant

Design outcomes

Primary

MeasureTime frame
Primary Outcome is to determine if correcting hypoalbuminemia with albumin infusion in post LT period, helps in decreasing the surgical drain output by 20% on post operative day 5Timepoint: Post Transplant Day 5

Secondary

MeasureTime frame
To compare the incidence of serious adverse events till dischargeTimepoint: Discharge date

Countries

India

Contacts

Public ContactVipul Gautam

Max centre for liver and biliary sciences

iam.vipulgautam@gmail.com9990833154

Outcome results

None listed

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