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ZIPS Study - Zip Incision Approximation vs. STAPLE

NCT02255877 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2016-10-24

No results posted yet for this study

Summary

Study designed to evaluate the Zip Surgical Skin Closure device versus conventional steel staple placement when utilized for surgical wound closure after bi lateral unicompartmental or bi later total knee replacement.

Conditions

  • Arthroplasty, Replacement, Knee

Interventions

DEVICE

Zip Surgical Skin Closure

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

DEVICE

Steel Staples

Skin Closure device for the closure of the skin layer for surgical incisions.

Sponsors & Collaborators

  • ZipLine Medical Inc.

    lead INDUSTRY

Principal Investigators

  • Eric Storne · VP Marketing

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2014-09-30
Completion
2014-09-30

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 NCT02255877 on ClinicalTrials.gov