MedTrace Logo

Study to Evaluate Clinical Efficacy and Safety of "Medifoam H" in Wound Healing

NCT01548443 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2013-02-06

No results posted yet for this study

Summary

The wound healing efficacy and safety of "Medifoam H" in patients with minor, acute trauma.

The hypothesis of this study is that using "Medifoam H" dressing for a week is not inferior to using "Duoderm THIN" dressing in wound healing.

Conditions

Interventions

DEVICE

Medifoam H dressing

Cover "medifoam H" on the wound for a week.

DEVICE

Duoderm THIN dressing

Cover "Duoderm THIN" on the wound for a week

Sponsors & Collaborators

  • The Catholic University of Korea

    collaborator OTHER

  • Seoul St. Mary's Hospital

    lead OTHER

Principal Investigators

  • Jong-Won Rhie, MD.,PhD · Seoul St. Mary's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • South Korea

Study Locations

More Related Trials

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 NCT01548443 on ClinicalTrials.gov