CTRI/2016/06/007032
Completed
Phase 2
Evaluation of Efficacy and Safety of AHPL/AYCAP/0413 capsule and AHPL/AYTOP/0213 cream in patients suffering from Acne Vulgaris - NI
Ari Healthcare Pvt Ltd0 sites63 target enrollmentTBD
ConditionsHealth Condition 1: null- Acne Vulgaris
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Acne Vulgaris
- Sponsor
- Ari Healthcare Pvt Ltd
- Enrollment
- 63
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Subjects suffering from acne vulgaris (mild, moderate and severe) as diagnosed by physician or dermatologist
- •2\. Subject willing to participate in clinical trial and who have read, understood and signed informed consent form.
- •3\. Subjects willing to make all required study visits
- •4\. Subjects willing to follow study instructions given by the investigator
Exclusion Criteria
- •1\.Patients with preexisting systemic disease necessitating long\-term medications.
- •2\.Patients with history of genetic and endocrinal disorders.
- •3\.Patients having menstrual disorders and patients with drug induced acne.
- •4\.Patients having systemic/topical treatment for acne vulgaris since last 3 months.
- •5\.Patients who are using any kind of face application for the management of acne.
- •6\.Patients suffering from major/severe illness(s).
- •7\.Patients having or given history of HIV, Hepatitis B or C, diabetes mellitus, hepatic/renal diseases and/or any other major skin disease(s).
- •8\.Pregnant and lactating women
- •9\.Subject having known hypersensitivity to any ingredient of investigational drugs .
- •10\.Subjects with significant abnormal laboratory parameters
Outcomes
Primary Outcomes
Not specified
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