Disposable Powered Articulating Linear Cutter Stapler in Total-Thoracoscopic Anatomic Lobectomy (Segmentectomy)

Lung Cancer Clinical Trial

Official title:

Clinical Trial on Performance and Safety of Disposable Powered Articulating Linear Cutter Stapler and Reloads in Total-Thoracoscopic Anatomic Lobectomy (Segmentectomy)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05329402
• Other study ID #: 20256031708-BC1
• Status: Completed
• Phase: N/A
• Start date: October 22, 2018
• Est. completion date: March 5, 2020

Study information

• Verified date: November 2023
• Source: Fengh Medical Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate whether the anastomosis success rate of the main effectiveness evaluation indexes is not inferior to the similar products produced by Johnson & Johnson when the Fengh Disposable Powered Articulating Endoscopic Linear Cutter Stapler Used for Thoracoscopic Anatomic Lobectomy (segmentectomy)

Description:

By comparing the effectiveness and safety of the disposable electric-endoscopic linear cutter stapler and cartridge (the subject product) produced by Jiangsu Fengh Medical Co., Ltd. and the similar product (electric-endoscopic linear cutter stapler with articulating head) produced by Johnson & Johnson in total-thoracoscopic anatomic lobectomy (segmentectomy), to prove that the subject product can be used for pulmonary tissue resection and anastomosis, and that the clinical trial meets the requirements of Good Clinical Practice for Medical Devices, Guidelines for Clinical Trial Design of Medical Devices and Guidelines for Technical Review of Endoscopic Stapler Registration, which can be used for product registration application.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 164
• Est. completion date: March 5, 2020
• Est. primary completion date: September 11, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Subjects aged 18-70 (inclusive), with no gender limitation;

2. The subject plans to undergo thoracoscopic anatomic pulmonary lobectomy (pulmonary segment);

3. Subjects or their guardians can understand the purpose of the study, show sufficient compliance with the study protocol, and sign the informed consent.

Exclusion Criteria:

1. Subjects have contraindications of video-assisted thoracoscopy;

2. The preoperative imaging results of the subjects indicated the presence of severe pleural adhesion and significant calcified hilar lymph nodes;

3. Subjects' platelet (PLT) <60x 10%/L or INR > 1.5;

4. Subjects forced expiratory volume in 1 second (FEV1)/expected value =50%, or forced expiratory volume in 1 second (FEV1)/use Vital capacity (FVC)=60%;

5. Cardiac ejection fraction =50%;

6. Major organ failure or other serious diseases (including clinically relevant cardiovascular diseases or within 12 months prior to enrollment) Myocardial infarction; A history of severe neurological or psychiatric illness; The presence of a serious infection before surgery that must be controlled with medication; Dissemination of activity Sexual intravascular coagulation; At high risk of blood clots);

7. The subject is a pregnant or lactating woman;

8. The subject participated in clinical trials of other drugs or devices within 1 month prior to the trial;

9. Other conditions that the researcher judged inappropriate for inclusion. .

Related Conditions & MeSH terms

• Lung Cancer

Intervention

Device:
• Disposable Powered Articulating Endoscopic Linear Cutter Stapler
Using the Disposable Powered Articulating Endoscopic Linear Cutter Stapler according to routine treatment
• ECHELON Flex Powered Articulating Endoscopic Linear Cutters
Using the ECHELON Flex Powered Articulating Endoscopic Linear Cutters according to routine treatment

Locations

Country	Name	City	State
China	Disposable Powered Articulating Endoscopic Linear Cutter Stapler	Jiangyin	Jiangsu

Sponsors (1)

Lead Sponsor	Collaborator
Fengh Medical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Anastomosis Success	The transection and anastomosis of lung tissues are performed during the operation. The device is withdrawn after successful triggering. The cutting staple line is carefully checked for integrity, air leakage and bleeding. If all staple lines are complete, without air leakage or bleeding, it is judged that the cutting and anastomosis of the device is successful. If there is persistent air leakage and bleeding at the anastomosis site, and conversion to thoracotomy is required, it is judged as device cutting and anastomosis failure.	During surgery