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Micropore Closure Kinetics at Various Body Sites

NCT03657277 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2021-07-28

Study results available
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Summary

The study to be performed will define the rate of skin barrier recovery following micropatch application to the skin on the upper arm, volar forearm, and abdomen in healthy subjects.

Conditions

  • Healthy

Interventions

DEVICE

Micropatch

Each micropatch contains 50 tiny projections (800 um in length)

Sponsors & Collaborators

  • University of Iowa

    lead OTHER

Principal Investigators

  • Nicole Brogden, PharmD, PhD · University of Iowa

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-10-01
Primary Completion
2020-03-18
Completion
2021-02-16

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 NCT03657277 on ClinicalTrials.gov