N/A N=160 Randomized Treatment

A Study Investigating the Efficacy of Various Wound Closure Devices in Reducing Postoperative Wound Complications

Joint Disease · Arthropathy

Bottom Line

View on ClinicalTrials.gov: NCT03134209 ↗

Enrolled (actual)

160

Serious AEs

1.3%

Results posted

Sep 2021

Primary outcome: Primary: Visual Analog Scale (VAS) for Pain — 4.53; 4.48; 4.54 score on a scale

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Zipper surgical skin closure (Device); Monocryl + Dermabond (Other); Polyester mesh + Dermabond (Other)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: NYU Langone Health
Primary completion: Aug 2020

Outcome Measures

Outcome	Result	p-value
PRIMARY Visual Analog Scale (VAS) for Pain	4.53; 4.48; 4.54	—

Summary

A single-center, phase IV, randomized, prospective study investigating the efficacy of various wound closure devices in reducing postoperative wound complications.

Eligibility Criteria

Inclusion Criteria

Patients who are undergoing joint arthroplasty

Exclusion Criteria

Treatment of total joint replacement surgery at an outside institution

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03134209). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.