Closure After Total Shoulder Arthroplasty: Prineo vs Dermabond

Status Terminated

Clinical Trial Summary

The objective is to compare two types of wound closure after total shoulder arthroplasty to determine which closure is faster, and subsequently if there are different outcomes between the two types of closures. The objective of this study is to compare two types of wound closure after total shoulder arthroplasty procedures. A single fellowship trained shoulder surgeon will perform all procedures. It is hypothesized that participants who undergo an 2-Octyl Cyanoacrylate (OCA) mesh closure will have a faster closure time, lower cost, non-inferior complication rate, and non-inferior satisfaction scores with respect postoperative follow up and scar appearance. Participants in the OCA mesh cohort will be compared to participants who have a closure with a running monocryl suture and dermabond. This investigation seeks to determine if OCA closure mesh closure is non-inferior to monocryl suture and dermabond in terms of operative time, cost, complications, and aesthetic appearance. If the hypothesis is confirmed, this study will suggest that a OCA mesh closure may be used for total shoulder arthroplasty surgeries as an alternative to current conventional closures and may provide a cost benefit.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Joint Diseases
Shoulder Arthritis
Shoulder Arthropathy Associated With Other Conditions

Clinical Trial Details

NCT number	NCT03899753
Study type	Interventional
Source	Montefiore Medical Center
Contact
Status	Terminated
Phase	N/A
Start date	December 31, 2020
Completion date	April 21, 2021

View Details

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