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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05257226
Other study ID # Bos study
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2019
Est. completion date December 31, 2030

Study information

Verified date February 2022
Source Kochi University
Contact Takehiro Okabayashi
Phone +81- 88-837-3000
Email tokabaya@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The evaluation for cancer treatment successful has been used by overall survival rate and/or postoperative complications, especially surgical area. Now postoperative QOL has been more importantly required. Therefore this study was conduced to investigate the association between postoperative outcomes and patients frailty.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 31, 2030
Est. primary completion date January 31, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - surgical 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
frailty
questionaire

Locations

Country Name City State
Japan Takehiro Okabayashi Kochi

Sponsors (1)

Lead Sponsor Collaborator
Kochi University

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative short-term outcomes postoperative complications up to 24 weeks
Secondary postoperative long-term outcomes survival rate 5 year
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