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A Prospective Randomized Controlled Trial to Compare Hemihepatic Vascular Inflow Occlusion, Portal Vein Inflow Occlusion and Pringle Maneuver in Partial Hepatectomy

A Prospective Randomized Controlled Trial to Compare the operative blood loss, postoperative liver function changees of Hemihepatic Vascular Inflow Occlusion, Portal Vein Inflow Occlusion and Pringle Maneuver in Partial Hepatectomy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000206224
Enrollment
180
Registered
2009-04-24
Start date
2006-10-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The impact of blood loss during liver resection and the need for perioperative blood transfusions have been shown to negatively impact perioperative morbidity and mortality as well as long term outcomes. The objective of this study is To compare the perioperative outcomes of partial hepatectomy using hemihepatic vascular inflow occlusion, portal vein inflow occlusion. and Pringle maneuver.

Interventions

Hemihepatic Vascular Inflow Occlusion group (In hemihepatic vascular inflow occlusion, the portal vein, hepatic artery, and bile duct were dissected in the hilum by lowering the liver plate. Either the right or left portal pedicle was isolated en bloc and was controlled with a tourniquet or Santinsky clamp. The estimated duration is around 30 minutes.) Portal Vein Inflow Occlusion group (In portal vein inflow occlusion, the portal vein was isolated and occluded with a tourniquet. The estimated d

Hemihepatic Vascular Inflow Occlusion group (In hemihepatic vascular inflow occlusion, the portal vein, hepatic artery, and bile duct were dissected in the hilum by lowering the liver plate. Either the right or left portal pedicle was isolated en bloc and was controlled with a tourniquet or Santinsky clamp. The estimated duration is around 30 minutes.) Portal Vein Inflow Occlusion group (In portal vein inflow occlusion, the portal vein was isolated and occluded with a tourniquet. The estimated duration is around 30 minutes.)

Sponsors

The Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

(1) Elective liver resection; (2) No other concomitant major surgical procedures, such as bowel or bile duct resection; (3) Compensated cirrhosis with Child-Pugh class A or B.

Exclusion criteria

1. Contralateral hepatic resection was required; 2. Total or selective vascular inflow/outflow occlusion was required because of tumor extent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026