Fact CheckerSign in

NCT07353489Completed

easyEndoTM Powered in Thoracic Surgery

Evaluation of the Safety and Efficacy of Single Use Powered Endoscopic Staplers and Cartridges in Thoracic Surgery: A Retrospective Clinical Study

Source: ClinicalTrials.gov · Last updated 20 Jan 2026

Brief summary (registry, in English)

The goal of this retrospective, single-arm is to evaluate the safety and performance of the easyEndo™ Powered Single Use Powered Endoscopic Staplers and Cartridges in thoracic surgery. The main question it aims to answer is the safety and performance of the staplers

Status (registry)
Completed
Study type
Interventional
Enrollment
61 (actual)
First submitted
12 Jan 2026
Start date
20 Nov 2025
Primary completion date
1 Jan 2026
Lead sponsor
Ezisurg Medical Co. Ltd.
NCT number
NCT07353489

What you commit to

  • Study type: Interventional
  • Participants enrolled: 61
  • From 20 Nov 2025 to the primary completion date, 1 Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who used other brands or types of endoscopic staplers instead of easyEndo™ Powered Single-Use Powered Endoscopic Staplers and Cartridges during surgery.
  • Surgery date was before January 1, 2024.
  • Patients with incomplete medical records or missing key information (e.g., unclear surgical procedures, unrecorded stapler use details, lost to follow-up before 1 year).

Other illness

  • Patients with severe underlying diseases that may affect postoperative outcomes or follow-up, such as end-stage heart, liver, or kidney disease, severe coagulation disorders, or uncontrolled malignant tumors (other than the primary disease requiring thoracic surgery).
  • Patients with allergies to the materials of easyEndo™ staplers or cartridges, or who experienced adverse reactions related to stapler material allergies intraoperatively or postoperatively.

Who the study is looking for

  • Patients who underwent thoracic surgery (including lobectomy, segmentectomy, wedge resection, etc.) using easyEndo™ Powered Single-Use Powered Endoscopic Staplers and Cartridges at our hospital.
  • Surgery date was on or after January 1, 2024.
  • Patients with complete medical records (including demographic data, surgical details, perioperative management, and follow-up information).
  • Patients who completed a 1-year postoperative follow-up, with available and valid follow-up data

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Affiliated Hospital of Jining Medical University
Coordinator of this site? Confirm its status
JiningChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.