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Feasibility Study of a Novel Device for Chronic Wounds

NCT00660049 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2017-12-13

Study results available
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Summary

The purpose of this study is to evaluate the feasibility and usability of a new portable and compact wound dressing device for the treatment of small chronic skin wounds.

Conditions

  • Ulcer
  • Wounds and Injuries

Interventions

DEVICE

SNaP Advanced Wound Care System

Application of negative pressure device daily per instructions

OTHER

SNaP

Daily use

OTHER

SNaP

Daily application per protocol

Sponsors & Collaborators

Principal Investigators

  • Dr. Anne Lynn S. Chang · Stanford University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2010-07-31
Completion
2010-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT00660049 on ClinicalTrials.gov