Open Versus Laparoscopic Left Hepatic Sectionectomy

Sponsor
The Second Hospital of Anhui Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03958825
Collaborator
(none)
88
1
2
45.7
1.9

Study Details

Study Description

Brief Summary

Laparoscopic left sectionectomy has been associated with shorter hospital stay and reduced overall morbidity compared with open left sectionectomy. Strong evidence has not, however, been provided.

Condition or Disease Intervention/Treatment Phase
  • Procedure: laparoscopic hepatic sectionectomy
  • Procedure: open left hepatic sectionectomy
N/A

Detailed Description

The application of laparoscopic technology to liver surgery has been developing rapidly, yet very few studies have been conducted to compare the outcomes between open and laparoscopic liver resections. So little is known about their advantages and disadvantages. The aim of this prospective randomized study is to compare the outcomes between laparoscopic and open liver resection in treatment of hepatolithiasis within the left lobes within an enhanced recovery after surgery programme.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
88 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
Randomized Clinical Trial of Open Versus Laparoscopic Left Hepatic Sectionectomy in Treatment of Hepatolithiasis Within an Enhanced Recovery After Surgery Programme
Actual Study Start Date :
Aug 10, 2019
Anticipated Primary Completion Date :
Dec 26, 2022
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: open left hepatic sectionectomy

patients undergoing open left hepatic sectionectomy within an enhanced recovery after surgery programme

Procedure: open left hepatic sectionectomy
patients undergoing open left hepatic sectionectomy within an enhanced recovery after surgery programme

Experimental: laparoscopic hepatic sectionectomy

patients undergoing a laparoscopic left hepatic sectionectomy within an enhanced recovery after surgery programme

Procedure: laparoscopic hepatic sectionectomy
patients undergoing a laparoscopic left hepatic sectionectomy within an enhanced recovery after surgery programme
Other Names:
  • open left hepatic sectionectomy
  • Outcome Measures

    Primary Outcome Measures

    1. Hospital duration after operation (days) [up to 30 days after liver resection]

      the length of hospital stay

    Secondary Outcome Measures

    1. Readmission percentage [up to 30 days after liver resection]

      Readmission percentage during one year follow-up

    2. Total morbidity [up to 1 year after liver resection]

      According to The Clavien-Dindo Classification, https://www.assessurgery.com/clavien-dindo-classification/

    3. Composite endpoint of liver surgery specific morbidity [up to 1 year after liver resection]

      Parameter composed of a combination of procedure-specific complications and considered as a single, dichotomous outcome: operative mortality, intra-abdominal haemorrhage, ascites, bile leakage, intra-abdominal abscess and postresectional liver failure. These components, which are all specific to liver surgery and have substantial clinical relevance, reflect Dindo grade 3-5 complications. A composite score of 1 (=failure) will reflect the occurrence of at least one of the above liver specific complications, consequently a score of 0 (=success) will be assigned if none occur.

    4. Hospital and societal costs [up to 1 year after liver resection]

      The economic evaluation will include a cost-utility analysis from a Dutch societal perspective. The incremental costs per Quality Adjusted Life Year (QALY) gained will be based on utility scores from the EQ-5D. All hospital expenses (direct and indirect) related to both interventions will be monitored. In addition, a cost questionnaire offered at the regular follow-up consultation (3, 6 and 12 months) will help us to assess the societal and individual costs outside health care relating to patients' absence, impaired mobility, work or normal daily activities.

    5. Incidence of incisional hernias [up to 1 year after liver resection]

      To assess the incidence of incisional hernias in laparoscopic and open left lateral hepatic sectionectomy patients will be contacted at a mean time of 1 year after resection to receive an ultrasound to diagnose incisional hernia.

    6. Change of serum glutamic oxalacetic transaminase [up to 7 days after liver resection]

      Change of serum glutamic oxalacetic transaminase after liver resection.These values will be recorded preoperative, and postoperative day-1,3,5,7.

    7. Change of serum glutamic-pyruvic transaminase [up to 7 days after liver resection]

      Change of serum glutamic-pyruvic transaminase after liver resection.These values will be recorded preoperative, and postoperative day-1,3,5,7.

    8. Mortality rates [up to 30 days after liver resection]

      the rate of postoperative death

    9. Operation time(min) [intraoperative]

      the during of operation

    10. Blood loss(ml) [up to 30 days after liver resection]

      the volume of blood loss

    11. Blood transfusion (times and units) [intraoperative]

      intraoperative blood transfusion

    12. C-reactive protein (mg/mL) [up to 5 days after liver resection]

      C-reactive protein levels on preoperative and postoperative day-1,3,5

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients suitable for undergoing both laparoscopic left sectionectomy as well as open left sectionectomy of the liver

    • Able to understand the nature of the study and what will be required of them

    • Men and non-pregnant,non-lactating women between age 18-80

    • BMI between 18-35

    • Patients with ASA I-II-III

    Exclusion Criteria:
    • Inability to give written informed consent

    • Patients undergoing liver resection other than left lateral hepatic sectionectomy

    • Patients with ASA IV-V Underlying liver disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The second hospital of Anhui Medical University, Hefei Anhui China 230061

    Sponsors and Collaborators

    • The Second Hospital of Anhui Medical University

    Investigators

    • Study Chair: hui hou, master, Second Affiliated Hospital of Anhui Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    hui hou, general surgery, The Second Hospital of Anhui Medical University
    ClinicalTrials.gov Identifier:
    NCT03958825
    Other Study ID Numbers:
    • 520
    First Posted:
    May 22, 2019
    Last Update Posted:
    Sep 18, 2020
    Last Verified:
    Sep 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Sep 18, 2020