CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 160 enrolled
Drug / intervention
Zipper surgical skin closure +2 moredevice
Likely dose
Zipper surgical skin closure deviceAI-extracted
Key inclusion· 1
  • Undergoing joint arthroplasty
Key exclusion· 1
  • Prior total joint replacement surgery at an outside institution

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03134209
NCT03134209N/ACompleted

A Single-center, Phase IV, Randomized, Prospective Study Investigating the Efficacy of Various Wound Closure Devices in Reducing Postoperative Wound Complications

NYU Langone Health·interventional·Posted Apr 28, 2017·Updated Sep 14, 2021

In Brief

A clinical study evaluating Zipper surgical skin closure, Monocryl + Dermabond, and 1 other intervention for Joint Disease and Arthropathy. Completed, enrolled 160 participants across 1 site.

Detailed Summary

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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedApr 28, 2017
Enrollment StartApr 26, 2017
Primary CompletionAug 31, 2020
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 9.2 years ago

Interventions

Zipper surgical skin closuredevice

The device acts like a scaffold to stabilize the adjacent sides of a wound in order to minimize forces that can disrupt normal healing of the skin.

Monocryl + Dermabondother

conventional sutures and skin adhesive glue

Polyester mesh + Dermabondother

conventional sutures and skin adhesive glue