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Evaluation of DermStream(tm) - an Irrigation Product for Chronic Wound Management

NCT00310752 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2008-08-01

No results posted yet for this study

Summary

The primary purpose of this study is to evaluate the safety of DermaStream(tm) in the management of chronic wounds.

Other goals of this study are to gain feedback from patients and healthcare providers on the ease of use (the ergonomic aspect) of the device, and to make a preliminary evaluation of the efficacy of DermaStream(tm) in chronic wound management.

Conditions

Interventions

DEVICE

DermaStream(tm) application and Streaming of Saline

Sponsors & Collaborators

  • EnzySurge

    lead INDUSTRY

Principal Investigators

  • Arie Bass, Prof. · Asaf Harofe Medical Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Primary Completion
2006-12-31
Completion
2006-12-31

Countries

  • Israel

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Entities

Diseases

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 NCT00310752 on ClinicalTrials.gov