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Clinical Performance and Safety of Suture-TOOL

Wound Infection Clinical Trial

Official title:
Clinical Performance and Safety of Suture-TOOL for Abdominal Wound Closure in Men and Women Patients Undergoing Elective Open Abdominal Surgery

Clinical Trial Summary

The goal of this single arm intervention study is to investigate the safety and performance of a suturing device for closure of the midline incision after open abdominal surgery. The study population consists of 38 patients selected for open abdominal procedures for malignant and benign colorectal disease. The main question it aims to answer is: • If the device facilitates a Suture-Length to Wound-Length (SL/WL) ratio of 4:1 Participants laparotomy wound will be closed with the device at the end of the operation and closure related data as closure time and SL/WL ratio will be calculated. The wound will be assessed for infection during the postoperative stay and the chart will be reviewed for wound dehiscence and wound infection.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05695157
Study type Interventional
Source Suturion AB
Contact Lena Toft, RN
Phone +46(0)424061570
Email lena.toft@skane.se
Status Recruiting
Phase N/A
Start date January 10, 2023
Completion date August 30, 2023
View Details
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