Clinical Trial on the Effects and Side Effects of ProOxy in the Treatment of Acne
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|ClinicalTrials.gov Identifier: NCT01682200|
Recruitment Status : Completed
First Posted : September 10, 2012
Last Update Posted : September 10, 2012
|Condition or disease||Intervention/treatment||Phase|
|Acne Vulgaris||Drug: ProOxy||Phase 1|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||50 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||An Open Label Pilot Clinical Trial on the Efficacy and Safety of ProOxy Facial Spray (Topical 15% Oxygen Solution) in the Treatment of Moderate Facial Acne Vulgaris Among Filipino Patients|
|Study Start Date :||October 2009|
|Actual Primary Completion Date :||March 2010|
|Actual Study Completion Date :||September 2011|
Experimental: ProOxy, Effects and Side Effects in treating acne
Patients are instructed to clean the face with ProOxy facial cleanser and then spray on the face wet enough but not dripping twice daily (upon waking up and before bedtime) for 3 months.
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.
Other Name: 15% Oxygen solution spray
- Changes in the appearances,sizes of the acne lesions as well as the disappearance of acne on the face. [ Time Frame: 4,8,12 weeks post application of the spray ]Upon acceptance,pictures are taken and acne lesions are identified and counted and after 4,8, and 12 weeks during and after application of ProOxy.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01682200
|Mary Chile General Hospital|
|Manila, Metro Manila, Philippines|
|Far Eastern University Hospital, Dept of Family Medicine|
|Quezon City, Metro Manila, Philippines|