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Clinical Trial Summary

Temporary portocaval Shunt during recipient hepatectomy improves intra operative parameters and morbidity in LDLT recipients


Clinical Trial Description

All patients satisfying the inclusion criteria, written informed consent will be taken and patients are randomized into intervention group ( Portocaval Shunt Group) and Non intervention group ( No Shunt Group).Patients from both the groups will be assessed for Hemodynamic parameters, Urine Output, Blood loss, blood products requirement , Duration of surgery during the procedure. They will be assessed for renal function, presence of sepsis, Morbidity, early graft dysfunction, ICU stay and total hospital stay in the post operative period.All patients will be followed up till discharge from hospital. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05385120
Study type Interventional
Source Institute of Liver and Biliary Sciences, India
Contact Manoj Kumar YL, MBBS, MS
Phone 9164313430
Email manojkumaryl91@gmail.com
Status Not yet recruiting
Phase N/A
Start date May 25, 2022
Completion date August 30, 2023

See also
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Not yet recruiting NCT06122792 - Preemptive TIPS for Gastric Variceal Bleeding in Patients With Cirrhosis N/A
Not yet recruiting NCT05128305 - Integrated Traditional Chinese and Clinical Medicine for Chronic Hepatitis B and Its Complication Phase 3