Skip to content

A clinical trial to compare the outcomes between two different liver grafts in recipients and donors after live donor liver transplantation

Randomized controlled trial to assess early post operative outcomes of Extended Right lobe grafts {with Middle Hepatic vein} versus Modified right lobe grafts{Reconstruction of segment 5 and segment 8 Branches} in the Recipient following Live Donor Liver Transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/08/007186
Enrollment
61
Registered
2016-08-16
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: null- To study the early post operative outcomes in patients who undergoe live donor liver transplantation as per standard accepted criteria.Outcome in donors who undergoe the donor surgery is also studied

Interventions

Intervention1: Extended Graft Group[Native middle hepatic vein]: Patients are randomized to groups were either the middle hepatic vein is taken from the donor or not. Intervention2: NIL: NIL Control I

Sponsors

Christi Titus Varghese
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: .Patients with liver disease who meet the criteria for live donor liver transplantation .Live donor suitable for extended right hepatectomy[with middle hepatic vein] a.Has a future liver remnant of more than 30% b.Live donor with adequate segment 4a drainage to left hepatic vein[usually a umblical vein] c.Steatosis less than 20% as assessed by L-S ratio on plain CT.

Exclusion criteria

Exclusion criteria: .Thrombosed recipient portal Vein. .Graft to recipient wight ratio less than 0.7. .Venous drainage of segment 4 mainly to middle hepatic vein in donor .ABO incompatible liver transplants .Donor at or above 55 years of age

Design outcomes

Secondary

MeasureTime frame
Change in post surgery liver parameters in donor and recipientTimepoint: Untill discharge/ 1Month [whichever comes later]

Primary

MeasureTime frame
Recipient: Early Allograft Dysfuction[EAD] Small for size Syndrome[SFSS] Primary graft non function[PGNF} Patency of Middle hepatic vein Number of days in ICU Mortality at the end of 90 days Donor: Post Hepatectomy liver failure[PHLF} Post operative Clavien-Dindo score Number of days in hospital after surgery CT based volume regeneration at the end of 60 daysTimepoint: All parameters uptil discharge/one month[which ever comes later] or as specified with the outcome.

Countries

India

Contacts

Public ContactChristi Titus Varghese

Amrita Institute Of Medical Sciences

sudhi@aims.amrita.edu9388623851

Outcome results

None listed

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