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Clinical Trial on the Effects and Side Effects of ProOxy in the Treatment of Acne

NCT01682200 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2012-09-10

No results posted yet for this study

Summary

This study was conducted to determine the effects and side effects of ProOxy facial spray in the treatment of acne.

Conditions

  • Acne Vulgaris

Interventions

DRUG

ProOxy

Clean the face with ProOxy facial wash before spraying ProOxy on the face enough to wet it twice daily, upon waking up and before bedtime.

Sponsors & Collaborators

  • Medivet Pty Ltd

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2010-03-31
Completion
2011-09-30

Countries

  • Philippines

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 NCT01682200 on ClinicalTrials.gov