Health Condition 1: Z526- Liver donor
Conditions
Interventions
Intervention1: Injection Pentoxifylline: Intravenous Pentoxifylline 1 mg/kg/hr dissolved in Plasma Lyte 12 hours before to 72 hours after Surgery
Control Intervention1: Intravenous Fluid (PLasmalyte/
Sponsors
Institute of Liver and Biliary Sciences
Eligibility
Inclusion criteria
Inclusion criteria: All Voluntary Healthy Liver Donors undergoing Right Lobe Donor Hepatectomy
Exclusion criteria
Exclusion criteria: Negative consent Hypersensitivity to pentoxifylline
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess effect of Pentoxifylline supplementation on Anatomical (Volume) Regeneration of liver in the Perioperative period (POD-14) in Right lobe donor HepatectomyTimepoint: On Post-operative Day-14 | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effect of Pentoxifylline on Liver function Tests- Time to NormalizationTimepoint: Baseline, POD- 1 to 7 and POD 14;To evaluate the effect of Pentoxifylline on biomarkers of liver regeneration (HGF, TNF-alpha, IL-6, TGF Beta, AFP)Timepoint: Baseline, POD-3 and POD-7;To study the effect of Pentoxifylline supplementation on post-operative complications in donor right hepatectomyTimepoint: Discharge from hospital | — |
Countries
India
Contacts
Public ContactParneet
Institute of liver and Biliary Sciences, New Delhi
Outcome results
None listed