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NCT05744362 Clinical Trial

Outcome of Transanal Specimen Extraction Surgery for Elderly Colorectal Cancer Patients

Colorectal Cancer Clinical Trial

Official title:
Outcome of Transanal Specimen Extraction Surgery for Elderly Colorectal Cancer Patients: a National Database Study in China of 1395 Cases

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05744362
Other study ID # KY2022-313
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2022
Est. completion date January 1, 2023

Study information
Verified date December 2022
Source The Second Affiliated Hospital of Harbin Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective analysis of a cohort of elderly CRC patients (aged ≥ 65 years) underwent transanal-NOSES between August 2008 and February 2022 was constructed. Data were obtained from China NOSES Database (CNDB). The primary outcomes included time to first flatus, postoperative hospital stays, 30-day postoperative complication and hospital mortality. The secondary outcomes were overall survival (OS) and disease-free survival (DFS).

Recruitment information / eligibility
Status Completed
Enrollment 1395
Est. completion date January 1, 2023
Est. primary completion date December 1, 2022
Accepts healthy volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: patients diagnosed as T1-4N0-2M0 colorectal cancer pathologically patients underwent transanal-NOSES patients aged 65 years or older Exclusion Criteria: patients with multiple primary colorectal cancer patients with total colectomy patients without complete data

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China The Second Affiliated Hospital of Harbin Medical University Harbin Heilongjiang

Sponsors (1)
Lead Sponsor Collaborator
The Second Affiliated Hospital of Harbin Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Overall survival Time of death from any cause after survival 4-year
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