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Zip® Surgical Skin Closure Device vs. Staples for Skin Closure in Subjects Having Undergone Bilateral Knee Arthroplasty

NCT02460172 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2019-03-05

Study results available
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Summary

Study designed to compare the Zip Surgical Skin Closure device vs. conventional staples for wound closure following bi lateral knee replacement surgery.

Conditions

  • Arthroplasty, Knee Replacement
  • Wound Healing

Interventions

DEVICE

Zip Surgical Skin Closure

Non invasive, reversible, skin closure device for closure of the skin layer following surgical incisions or laceration repair.

DEVICE

Steel Staples

Skin closure device for the closure of the skin layer following surgical incision

Sponsors & Collaborators

  • ZipLine Medical Inc.

    lead INDUSTRY

Principal Investigators

  • Rodney Benner, MD · Study Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2017-02-15
Completion
2017-02-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02460172 on ClinicalTrials.gov