MedTrace Logo

Evaluation of a Novel Post-Surgical Dressing

NCT01831596 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 59

Last updated 2024-11-25

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate the safety and efficacy of the Closed-Incision SNaP Device.

Conditions

  • Post Surgical Wound

Interventions

DEVICE

ciSNaP

SNaP disposable, mechanically powered Negative Pressure Wound Therapy System

Sponsors & Collaborators

  • 3M

    collaborator INDUSTRY

  • KCI USA, Inc

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2012-06-30
Completion
2012-06-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT01831596 on ClinicalTrials.gov