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A Study to Assess Wound Healing Efficacies of Different Adhesive Bandages

NCT04040933 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2023-07-03

Study results available
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Summary

The purpose of this study is to assess the wound healing efficacy (time to complete healing) of different adhesive bandages.

Conditions

  • Wound Healing

Interventions

DEVICE

Marketed Adhesive Bandage #1

On the randomized wound site, a marketed adhesive bandage will be applied.

DEVICE

Marketed Bandage #2

On the randomized wound site, a marketed adhesive bandage will be applied.

DEVICE

Non-Marketed Bandage #1

On the randomized wound site, a non-marketed adhesive bandage will be applied.

DEVICE

Non-Marketed Bandage #2

On the randomized wound site, a non-marketed adhesive bandage will be applied.

DEVICE

Non-Marketed Adhesive Bandage #3

On the randomized wound site, a non-marketed adhesive bandage will be applied.

DEVICE

Non-Marketed Adhesive Bandage #4

On the randomized wound site, a non-marketed adhesive bandage will be applied.

DEVICE

Non-Marketed Adhesive Bandage #5

On the randomized wound site, a non-marketed adhesive bandage will be applied.

Sponsors & Collaborators

  • Johnson & Johnson Consumer Inc. (J&JCI)

    lead INDUSTRY

Principal Investigators

  • Lily Jiang, PhD · Thomas J. Stephens & Associates, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2019-08-09
Primary Completion
2019-10-18
Completion
2019-10-30
FDA Device
Yes

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 NCT04040933 on ClinicalTrials.gov