Skinpen Precision System for Vitiligo

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
VitiligoSkinpen Precision System - Device
Eligibility
18 - 60
All Sexes
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Study Summary

This study is evaluating whether microneedling is an effective treatment for vitiligo.

Treatment Effectiveness

Effectiveness Progress

1 of 3

Study Objectives

1 Primary · 1 Secondary · Reporting Duration: Through Study Completion, over the course of 244 days

Day 244
Physician's Global Assessment (PGA)
Subject's assessment of their pre and post-treatment images using the Vitiligo Noticeability Scale (VNS)

Trial Safety

Trial Design

1 Treatment Group

Microneedling with Skinpen Precision System
1 of 1

Experimental Treatment

10 Total Participants · 1 Treatment Group

Primary Treatment: Skinpen Precision System · No Placebo Group · N/A

Microneedling with Skinpen Precision System
Device
Experimental Group · 1 Intervention: Skinpen Precision System · Intervention Types: Device

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: through study completion, over the course of 244 days

Who is running the clinical trial?

Crown Laboratories, Inc.Lead Sponsor
3 Previous Clinical Trials
129 Total Patients Enrolled

Eligibility Criteria

Age 18 - 60 · All Participants · 7 Total Inclusion Criteria

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Who else is applying?

What state do they live in?
Indiana100.0%
How old are they?
18 - 65100.0%
What site did they apply to?
Crown Laboratories100.0%
What portion of applicants met pre-screening criteria?
Met criteria100.0%