Not Yet Recruiting
OBSERVATIONAL
NCT06677008
Post-market Clinical Follow-up Study Plan for Disposable Endoscopic Linear Cutter Stapler
View on ClinicalTrials.gov
Updated Dec 15, 2025
Brief Summary
This study conducted a Post-Market Clinical Follow-Up study (PMCF) to evaluate the safety and effectiveness of the disposable endoscopic linear cutter stapler produced by Changzhou Ankang Medical Instrument Co., Ltd., through a retrospective analysis of the clinical data, to evaluate the safety and effectiveness of soft tissue resection, transection and anastomosis.
Interventions
Name:
Disposable endoscopic linear cutter stapler
Type:
DEVICE
Description:
Investigational devices of all the models of the staplers and its cartridge listed in Study Plan(Plan number: CAK-PMCF)
Primary Outcomes
Measure:
Anastomosis success rate
TimeFrame:
the investigation sites will be collected from January 2023 to September 2024.
Description:
The condition of no reoperation in situ was defined as successful anastomosis as determined by surgical records and hospitalization medical records.
Trial Information
NCT ID
NCT06677008
Status
Not Yet Recruiting
Study Type
OBSERVATIONAL
Sponsor
Suzhou Kerui Medical Technology Co., Ltd
Last Updated
December 15, 2025