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Clinical Trials/CTRI/2018/11/016315
CTRI/2018/11/016315
Recruiting
未知

Randomized Controlled Trial to compare Early Postoperative Outcomes of Polytetrafluoroethylene Graft Vs. Native Recipient Portal Vein fro Middle Hepatic Vein Reconstruction in the Recipient following Live Donor Liver Transplantation - RePoVer Trial

Amrita Institute of Medical Sciences Research Centre0 sites0 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Amrita Institute of Medical Sciences Research Centre
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •ADULT to ADULT LIVE DONOR LIVER TRANSPLANT PATIENTS with Decompensated Liver Disease (Acute/Subacute/Chronic)
  • •Live Donor suitable for Right lobe donation with
  • •1\. Functional Liver Reserve \> 30%
  • •2\. Adequate Segment 4 drainage to the Left Hepatic Vein
  • •3\. Steatosis \< 20% assesses by Plain CT

Exclusion Criteria

  • •PORTAL VEIN THROMBOSIS IN THE RECIPIENT
  • •HEPATOCELLULAR CARCINOMA IN THE RECIPIENT
  • •ABO Incompatible Transplants
  • •DONOR \- TYPE II or TYPE III Portal vein anatomy

Outcomes

Primary Outcomes

Not specified

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