Relationship Between Liver Cancer and Sarcopenia

Sponsor
First Affiliated Hospital of Wenzhou Medical University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05339919
Collaborator
Qilu Hospital of Shandong University (Other), The Second Hospital of Shandong University (Other)
1,200
1
63.9
18.8

Study Details

Study Description

Brief Summary

By tracking the short-term and long-term results of patients after hepatectomy, the difference of short-term results between patients with sarcopenia and patients without sarcopenia was analyzed, and the correlation between sarcopenia and short-term and long-term results of patients after hepatectomy was explored, so as to improve people's awareness of sarcopenia and pay attention to its prevention and treatment.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: gait speed; ct scan;grip strength and chair stand test

Detailed Description

All implementation details are based on the newest EWGSOP definition. The investigators consecutively admitted patients the questionnaire and evaluated the assessment of muscle strength (grip strength test and chair stand test), muscle quantity (L3 plane total skeletal muscle area) and physical performance (gait test) following the F-A-C-S approach, to confirm patients with sarcopenia accurately. And by tracking the short-term and long-term outcomes of patients after hepatectomy, the differences were analyzed and the relationship between sarcopenia and liver cancer was explored.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
1200 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
The Effect of Sarcopenia on Hepatocellular Carcinoma After Hepatectomy
Actual Study Start Date :
May 1, 2020
Actual Primary Completion Date :
Aug 11, 2021
Anticipated Study Completion Date :
Aug 28, 2025

Outcome Measures

Primary Outcome Measures

  1. Short-term postoperative results [3 months]

    Postoperative complications;90 days readmission rate

  2. Long-term results after operation [10 years]

    Overall survival; Disease free survival

Secondary Outcome Measures

  1. Postoperative hospitalization time [2 months]

    Time window from the day of operation to the day of discharge.

  2. Hospitalization expenses [2 months]

    All hospitalization expenses, including drug expenses, operation expenses, anesthesia expenses, nursing expenses and other expenses.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with preoperative clinical diagnosis of liver cancer

  • No cancer other than liver cancer has been diagnosed

  • Age ≥18 years

Exclusion Criteria:
  • Patients who could not complete the standard tests and questionnaires

  • Patients who did not accept liver resection after evaluation of treatment plan

  • Patients who had other concomitant preoperative causes of muscle weakness (injury, fracture, stroke, etc.)

  • Patients who missing CT data or CT scan did not reach the level of the third lumbar vertebra (L3)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gang Chen Wenzhou Zhejiang China 325000

Sponsors and Collaborators

  • First Affiliated Hospital of Wenzhou Medical University
  • Qilu Hospital of Shandong University
  • The Second Hospital of Shandong University

Investigators

  • Principal Investigator: Gang Chen, M.D., First Affiliated Hospital of Wenzhou Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gang Chen, MD, Clinical Professor, Principal Investigator, First Affiliated Hospital of Wenzhou Medical University
ClinicalTrials.gov Identifier:
NCT05339919
Other Study ID Numbers:
  • sarcopenia
First Posted:
Apr 21, 2022
Last Update Posted:
Jun 15, 2022
Last Verified:
Jun 1, 2022
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
Keywords provided by Gang Chen, MD, Clinical Professor, Principal Investigator, First Affiliated Hospital of Wenzhou Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 15, 2022