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Site for A RANDOMIZED, DOUBLE-BLIND, MULTI-CENTER COMPARATIVE EFFECTIVENESS STUDY OF SPIRONOLACTONE VERSUS DOXYCYCLINE HYCLATE FOR THE TREATMENT OF ACNE IN WOMEN

Mild to Severe Acne: Women ages 16-40 years. Assigned to either spironolactone of doxycycline; oral medication taken once daily. The duration of the study will last 16 weeks. During that time participants will attend 3 in person study visits (study start, week 8 and week 16). In addition participants will completion questions outside of study visits at Week 4 and Week 12. The goal of this trial is to compare the effectiveness of spironolactone and doxycycline hyclate in the treatment of acne in women.

The duration of the study will last 16 weeks. During that time participants will attend 3 in person study visits (study start, week 8 and week 16). In addition participants will completion questions outside of study visits at Week 4 and Week 12.

Joslyn Kirby
Amy Longenecker - at alongenecker@pennstatehealth.psu.edu or 717-531-5136
 

Female
All
This study is NOT accepting healthy volunteers
NCT04582383
SITE00001097
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Inclusion Criteria:
Assigned female at birth; ages 16-40 years old
Birth control options will be discussed by study coordinator
Exclusion Criteria:
Certain acne treatments are not allowed; study coordinator will discuss
Certain medical history conditions are not allowed; study coordinator will discuss
Skin Conditions
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See this study on ClinicalTrials.gov
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Location Contacts
Hershey, PA ,