Health Condition 1: K746- Other and unspecified cirrhosis ofliver Health Condition 2: null- Patients with chronic liver disease undergoing live donor liver transplantation and their donors(As recipient-donor pairs) are included in the study
Conditions
Interventions
Intervention1: N-ACETYLCYSTEINE: infusion during donor hepatectomy(In donor) and recipient surgery(in recipient) and also during post-operative period for 96 hours in recipient
Control Intervention1:
Sponsors
MOHAMED ABDULLATHEEF TK
Eligibility
Inclusion criteria
Inclusion criteria: All Living donor pairs undergoing liver transplantation during the period of study who are willing to participate in the study.
Exclusion criteria
Exclusion criteria: 1. ABO incompatible liver transplants 2. Liver transplantations in which the recipient age is less than 18
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Initial Poor Graft functionTimepoint: 5 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Hepatic artery or portal vein thrombosisTimepoint: Any time during 30 days after liver transplantation;Length of ICU stayTimepoint: Duration of ICU stay;Liver enzymesTimepoint: peak levels of AST and ALT within the first 7 postoperative days;MortalityTimepoint: 30 days;Post operative bleedingTimepoint: Within 24 hours;Primary non-functionTimepoint: 10 days;Prothrombin time and INRTimepoint: preoperative, postoperative at day 5 and day 10, peak and median level over the first 14 postoperative days;Serum bilirubinTimepoint: preoperative, postoperative at day 5 and day 10, peak and median level over the first 14 postoperative days;Serum creatinineTimepoint: preoperative, postoperative at day 5 and day 10, peak and median level over the first 14 postoperative days;Significant renal Function deterioration deteriorationTimepoint: Within 30 days of Liver transplantation | — |
Countries
India
Contacts
Public ContactMOHAMED ABDULLATHEEF T K
Sudhamayi Hospitals and Clinics
Outcome results
None listed