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LiquiBand® Exceed™ and LiquiBand® Rapid™ for General Surgery Procedures — Exceed  

Surgical Wound Clinical Trial

Official title:
Clinical Study to Evaluate LiquiBand® Exceed™ and LiquiBand® Rapid™ for Closure of Surgical Incisions Associated With Abdominal Surgery

Clinical Trial Summary

The purpose of this post market study is to evaluate the performance and safety of LiquiBand® Exceed™ and LiquiBand® Rapid™ for closure of surgical incisions associated with abdominal surgery.

Clinical Trial Description

LiquiBand® Exceed™ and LiquiBand® Rapid™ are the "study" devices. The study devices are an adhesive used to close surgical wounds. When the adhesive is applied to the skin, it polymerizes (forms a chemical bond) within minutes due to the moisture on the skin's surface and allows the wound edges to remain in the correct position. The use of the study devices are not "investigational" (experimental) because it is already cleared for doctors to use for surgical wound closure in the United States of America. In this study, LiquiBand® Exceed™ and LiquiBand® Rapid™ will be used to close surgical wounds following general abdominal surgery. Subjects will be followed up for 14-days post surgery, and safety and performance of the study device will be evaluated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04740775
Study type Interventional
Source Advanced Medical Solutions Ltd.
Contact Tina Warburton
Phone 01606 863500
Email tina.warburton@admedsol.com
Status Recruiting
Phase N/A
Start date November 8, 2022
Completion date April 2024
View Details
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