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Altrazeal Range of Motion Study Comparing With Typical Carboxymethyl

NCT01062191 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2011-06-08

No results posted yet for this study

Summary

The objective of this study is to evaluate the difference in joint range of motion of a new flexible hydrogel nanoparticle wound dressing compared to typical sodium carboxymethylcellulose dressing Aquacel AG for treatment of partial thickness burns.

Conditions

  • Burn

Interventions

DEVICE

Aquacel AG, typical carboxymethylcellulose dressing

4" X 4", Aquacel silver sheet

DEVICE

Altrazeal Flexible Hydrogel Nanoparticle Wound Dressing

Wound dressing

Sponsors & Collaborators

  • ULURU Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
2 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2008-10-31
Completion
2008-10-31

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 NCT01062191 on ClinicalTrials.gov