Actively Recruiting

Age: 18Years - 85Years
All Genders
NCT07452848

Impact of Pringle Maneuver on Postoperative Gallbladder Diseases After Hepatectomy

Led by West China Hospital · Updated on 2026-03-05

2000

Participants Needed

8

Research Sites

21 weeks

Total Duration

On this page

Sponsors

W

West China Hospital

Lead Sponsor

F

First Affiliated Hospital of Harbin Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The liver is an organ with a rich blood supply. During liver surgery (hepatectomy), surgeons often temporarily clamp the blood vessels supplying the liver to maintain a clear surgical field and reduce bleeding. This common technique is known as the Pringle maneuver. However, this maneuver also temporarily cuts off the blood supply to the gallbladder. Currently, doctors debate whether to routinely remove a healthy gallbladder during liver surgery to prevent future gallbladder problems, or to preserve it. The primary purpose of this multicenter retrospective cohort study is to evaluate whether using the Pringle maneuver during liver surgery increases the risk of patients developing gallbladder diseases (such as gallstones or inflammation) later on. Researchers will review the past medical records of patients who underwent liver surgery with their gallbladder preserved between January 2012 and January 2022. By comparing patients who had the Pringle maneuver with those who did not, the study aims to provide reliable clinical evidence to help surgeons make better decisions about whether to preserve or remove the gallbladder during liver surgery.

CONDITIONS

Official Title

Impact of Pringle Maneuver on Postoperative Gallbladder Diseases After Hepatectomy

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 85 years
  • Definite diagnosis of hepatic solid lesions confirmed by imaging or pathology
  • Underwent elective hepatectomy with gallbladder preservation
  • Preoperative liver function classified as Child-Pugh class A or B
  • Preoperative physical status classified as ASA class I, II, or III
Not Eligible

You will not qualify if you...

  • Preexisting biliary tract diseases such as gallstones, biliary inflammation, or tumors
  • History of previous upper abdominal surgery
  • Use of non-hepatic inflow occlusion methods during surgery
  • Long-term use of hormone replacement therapy, somatostatin or its analogues, or oral contraceptives
  • Loss to follow-up or missing important postoperative data

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 8 locations

1

The First Affiliated Hospital of University of Science and Technology of China

Hefei, Anhui, China

Actively Recruiting

2

Xinqiao Hospital of Army Medical Universit

Chongqing, Chongqing Municipality, China

Actively Recruiting

3

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China

Actively Recruiting

4

Zhujiang Hospital of Southern Medical University

Guangzhou, Guangdong, China

Actively Recruiting

5

The First Affiliated Hospital of Harbin Medical University

Harbin, Heilongjiang, China

Actively Recruiting

6

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China

Actively Recruiting

7

Nanjing Drum Tower Hospital

Nanjing, Jiangsu, China

Actively Recruiting

8

Tianjin Medical University Cancer Institute and Hospital

Tianjin, Tianjin Municipality, China

Actively Recruiting

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Research Team

J

Jiwei Huang

CONTACT

J

Jun Ji

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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