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ROLE OF VITAMIN C IN IMPROVING THE RESULTS OF LIVING DONOR LIVER TRANSPLANTATION

Efficacy of intravenous ascorbic acid in reducing the incidence of reperfusion syndrome in adult living donor liver transplantation – a randomised double blinded placebo controlled trial. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097179
Enrollment
40
Registered
2025-11-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: K74- Fibrosis and cirrhosis of liver Health Condition 2: K740- Hepatic fibrosis

Interventions

Intervention1: Ascorbic acid: 1. Treatment group-3gm of ascorbic acid diluted in 100 ml of 0.9% saline solution will be administered intravenously during the start of graft implantation and post opera

Sponsors

V M NAVEEN RAJ
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult living donor liver transplant recipients willing to take part in the study.

Exclusion criteria

Exclusion criteria: 1. Renal dysfunction due to calcinosis. 2. Unresolving HRS. 3. Known Allergy to ascorbic acid 4. Glucose-6-phosphate dehydrogenase (G6PD) deficiency 5. Hyperoxaluria 6. Hyperuricemia 7. Haemochromatosis 8. ABOi transplants

Design outcomes

Primary

MeasureTime frame
Reduction in the incidence of reperfusion syndrome following adult living donor liver transplantation with Ascorbic acid infusion after the start of graft implantationTimepoint: Intra-operative duration of liver implantation-5 minutes after reperfusion.

Secondary

MeasureTime frame
1. Dose of vassopressors during the time of reperfusion 2. Thromboelastogram 3. Blood Products requirement after reperfusion 4. Rates of early graft dysfunction & PNF (Olthoff criteria) 5. Length of ICU & Hospital stay 6. Development of postoperative kidney failure (acute kidney injury [AKI]) during the first week. 7. Time zero biopsy of the graft after reperfusion 8. Proinflammatory cytokines levels after reperfusion (IL-1, IL-2, IL-8 & TNF-a Timepoint: 4 weeks

Countries

India

Contacts

Public ContactDR S SUDHINDRAN

Amrita Institute of medical sciences

sudhisalini@icloud.com9388623851

Outcome results

None listed

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