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Recruiting

NCT Number: NCT05257434

Postoperative Outcomes in Patients With Hepato-biliary-pancreatic Cancer According to inBody Test

postoperative outcomes were evaluated by using inBody test

Recruiting

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Key information

Conditions

Cancer Neoplasms

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

postoperative outcomes were evaluated by using inBody test

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • surgically treated patients

Exclusion criteria

  • a body weight loss of >10% during the 6 months before surgery; the presence of distant metastases; or seriously impaired function of vital organs because of respiratory, renal, or heart disease

Treatment and study plan

inbody

Behavioral

Body fluid composition

Primary outcomes

  1. long-term outcomes

    Time frame: 5year

    overall survival rate

Secondary outcomes

  1. short-term outcomes

    Time frame: up to 24 weeks

    postoperative complications

Sponsors and collaborators

Lead sponsor

Kochi University

Other

Registry information

Important dates

Study start
2019
Primary completion
2025
Study completion
2030
First posted
Feb 25, 2022
Registry last updated
Feb 25, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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