Skip to content

To Compare the Outcome of Temporary Portocaval Shunt During Recipient Hepatectomy Versus No Shunt in Adult Elective Live Donor Liver Transplantation.

To Compare the Outcome of Temporary Portocaval Shunt During Recipient Hepatectomy Versus No Shunt in Adult Elective Live Donor Liver Transplantation- A Prospective Randomised Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05385120
Enrollment
40
Registered
2022-05-23
Start date
2022-05-25
Completion date
2023-08-30
Last updated
2022-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Portosystemic Shunt

Keywords

Temporary Portocaval shunt, Recipient Hepatectomy, Liver transplantation

Brief summary

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

Detailed 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.

Interventions

In Temorary Portocaval Shunt Group (TPCS group), Hilar dissection( division of Hepatic artery, Bileduct) is followed by temporary portocaval shunt formation during recipient Hepatectomy.

Sponsors

Institute of Liver and Biliary Sciences, India
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

A Randomised Pilot study

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1\) All Adult LDLT Recipients at ILBS, New Delhi

Exclusion criteria

1. Acute Liver Failure as an indication for transplant 2. Pediatric transplants 3. Presence of Yerdel grade III and grade IV Portal vein thrombosis 4. Presence of significant portosystemic shunting (greater than 10mm) in pre operative period. 5. Patients who have undergone TIPS procedure. 6. Hypercoagulable states like Budd-Chiari syndrome 7. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Urine output between two groupsDuring Transplantation procedureUrine output during the transplantation procedure is measured in milliliter
Blood Pressure between two groups at fixed time pointsT0- At the beginning of the procedureSystolic Blood pressure, Diastolic Blood Pressure and Mean Blood Pressure is measured in mmHg
Ionotropes requirement between two groups at fixed time pointsT0- At the beginning of the procedureNoradrenaline and Vasopressin requirement in milliliter/hour
Lactate level between two groups at fixed time pointsT0- At the beginning of the procedureLactate levels are documented from Arterial Blood Gas analysis
Blood loss between two groups during intraoperative periodDuring ProcedureBlood loss during the procedure is measured in milliliter
Duration of surgery between two groups.During ProcedureDuration between incision time to closure of abdomen is noted in minutes
Increase in creatinine levels of Increase 1.5-1.9 times from baseline in the post op period.Number of days post transplantation procedure (upto 45 days)Serum Creatinine is measured in milligram per deciliter
≥0.3 mg/dl increase within 48 h or Urine output < 0.5 ml/kg/h for 6-12 h in the post op period.Number of days post transplantation procedure (upto 45 days)Serum Creatinine is measured in milligram per deciliter

Secondary

MeasureTime frameDescription
Endotoxin levelsLevels of Serum endotoxin levels in pre op and 12 hours after surgerySerum endotoxin levels increases in cases of bowel congestion and hemodynamic instability when portal vein is clamped during recipient hepatectomy
Number of patients with Early allograft dysfunctionFor 5 consecutive days after day 7Early allograft dysfunction using criteria defined - total bilirubin \>10 mg/dL, INR \>1.6 and serum urea \>100 mg/dL, for five consecutive days after day 7
Incidence of MorbidityNumber of days post transplantation procedure (upto 45 days)Morbidity is defined by Clavein Dindo Classification - \>/=3. Sepsis as defined by Sepsis- 3 criteria, presence of 2 or more of the following 1.altered mentation, 2.respiratory rate ≥22 breaths/min 3.systolic blood pressure ≤100 mm Hg
Incidence of sepsisNumber of days post transplantation procedure (upto 45 days)Morbidity is defined by Clavein Dindo Classification - \>/=3. Sepsis as defined by Sepsis- 3 criteria, presence of 2 or more of the following 1.altered mentation, 2.respiratory rate ≥22 breaths/min 3.systolic blood pressure ≤100 mm Hg
Number of days of ICU stayNumber of days post transplantation procedure (upto 45 days)Day patient shifted from ICU to ward is documented as total ICU stay. Day patient is discharged from hospital is documented for total hospital stay
Number of days of hospital stayNumber of days post transplantation procedure (upto 45 days)Day patient shifted from ICU to ward is documented as total ICU stay. Day patient is discharged from hospital is documented for total hospital stay
To compare tolerance to enteral feed between two groupsNumber of days post transplantation procedure (upto 45 days)Tolerance to NG feed is defined by absence of bloating, nausea, vomiting, abdominal distention or ileus

Contacts

Primary ContactManoj Kumar YL, MBBS, MS
manojkumaryl91@gmail.com9164313430

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026