Clinical Trial on the Effects and Side Effects of ProOxy in the Treatment of Acne (NCT01682200) | Clinical Trial Compass
CompletedPhase 1
Clinical Trial on the Effects and Side Effects of ProOxy in the Treatment of Acne
Philippines50 participantsStarted 2009-10
Plain-language summary
This study was conducted to determine the effects and side effects of ProOxy facial spray in the treatment of acne.
Who can participate
Age range18 Years – 40 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
What they're measuring
1
Changes in the appearances,sizes of the acne lesions as well as the disappearance of acne on the face.
Timeframe: 4,8,12 weeks post application of the spray