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

• Status: Completed
• Trial end date: 2011-09-01
• Target enrollment: 0
• Participant gender: All

Summary

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

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Medivet Pty Ltd

Criteria

Inclusion Criteria:

• patients with acne on their faces only

• patients who are at least 18 years of age

• patients who have normal and disease free skin at the dorsal surface of the upper arm.

• patients who are willing to follow instructions on both the Patch Test Part one and Part Two procedures and to follow scheduled visits.

Exclusion Criteria

• patients with systemic illnesses(such as but not limited to heart disease, hypertension, diabetes, cancer, liver disease, kidney disease)

• patients with very dark skin color, Fitzpatrick skin type V-VI, who are prone to post=inflammatory hyperpigmentation.

• patients with intake of oral medications including glucocorticoids or any immuno-suppressants or who have undergone ultraviolet phototherapy for the past 2 weeks prior to the patch test.

• patients with history of contact dermatitis, dermatographism or anaphylaxis.

• patients with history of eczematous and inflammatory dermatitis, seborrheic dermatitis and psoriasis.