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Visualizing Dermal Micropores With OCT

NCT04867733 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 49

Last updated 2024-05-28

Study results available
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Summary

The study to be performed will allow visualization of skin micropores following microneedle treatment in healthy subjects in differing racial/ethnic backgrounds.

Conditions

  • Healthy

Interventions

OTHER

Micropatch (microneedle patch)

Each micropatch contains an array of 50 microneedles.

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
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2022-06-29
Completion
2022-06-29

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 NCT04867733 on ClinicalTrials.gov