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A Test of Different Kinds of Bandages on Healing of Wounds

NCT01770860 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2014-08-04

Study results available
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Summary

This two-week study will compare the healing of minor wounds when no bandage is applied against four different types of bandages.

The study investigators will make five small wounds similar to scrapes (about a half-inch square) on the back of subjects who qualify to participate in the trial and have given informed consent. Four of the wounds will be covered by different bandages and one will be left uncovered. Participants will visit the clinic every day for 2 weeks or until all the wounds are healed (whichever comes first). At the clinic, the bandages will be removed, the doctor will score the wounds, a picture will be taken of the wounds and new bandages will be applied.

It is expected that some pain and itching will be experienced, because they are part of the normal wound healing process. Subjects will be asked about adverse events at each visit and will have the opportunity to discuss issues or concerns with the investigator or the doctor during the course of the trial. It is expected that the wounds will be completely healed within 14 days, but if not, the participant will need to return to the clinic for follow-up treatment until the wounds are completely healed.

We will see if the different bandages help with the healing of the wounds during the study.

Conditions

  • Wound Healing

Interventions

DEVICE

6660

At each daily visit, designated study personnel will replace the specific test product on the assigned wound site.

DEVICE

4314

At each daily visit, designated study personnel will replace the specific test product on the assigned wound site.

DEVICE

8336

At each daily visit, designated study personnel will replace the specific test product on the assigned wound site.

DEVICE

4840

At each daily visit, designated study personnel will replace the specific test product on the assigned wound site.

Sponsors & Collaborators

  • Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies, Inc.

    lead INDUSTRY

Principal Investigators

  • Clare Kendall · Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies, Inc.

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-02-28
Completion
2013-02-28

Countries

  • United States

Study Locations

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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 NCT01770860 on ClinicalTrials.gov