CTRI/2019/03/018138CompletedPhase 4
A Clinical study to evaluate the effectiveness of study face wash in subjects with acne vulgaris(Mukhadooshika).
Ramaiah Indic Specialty Ayurveda0 sites50 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Male and female volunteers, with age 18â??45 years
- •2. Subjects willing and able to provide informed consent voluntarily
- •3. Subjects with facial acne grade of I-III as assessed by Investigatorâ??s Global Assessment
- •4. Willing to maintain the investigational product use throughout the study.
- •5. Subjects who have not undergone any skin therapy in last 3 months
- •6. Subjects with no known allergy to any of the test ingredients
- •7. Women using oral contraceptives must have been doing so for at least 6 consecutive months prior to entering the study, and are required to continue with the same brand throughout the study period
- •8. Subjects who are willing to refrain from using any skin care product other than the investigational product, like, moisturizers, face washes and face creams, for the duration of the study
- •9. Subjects willing and able to comply with all trial requirements
- •10. Laboratory workup within normal limits; including complete hemogram, glucose, blood urea nitrogen, creatinine, liver function test, lipid profile, thyroid-stimulating hormone, urine pregnancy test
Exclusion Criteria
- •1. Subjects who have skin diseases like psoriasis, atopic dermatitis etc. at the time of screening
- •2. Subject with chronic systemic illnesses or treatment that can affect skin health eg. Polycystic ovarian disease
- •3. Subjects on oral medications or suffering from chronic illness which will compromise the study
- •4.Women who have stopped using oral contraceptives less than three months prior to entering the study
- •5. Subjects who have participated in a similar investigation in the past four weeks
- •6. Pregnant or lactating women
Investigators
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