CTRI/2023/08/056537
Recruiting
Phase 4
A single blind clinical study to evaluate the effectiveness and Safety of Plum Vitamin C serum for skin brightening. - NI
Pureplay skin sciences0 sites0 target enrollmentTBD
ConditionsHealth Condition 1: L700- Acne vulgaris
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: L700- Acne vulgaris
- Sponsor
- Pureplay skin sciences
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Gender: Non\-pregnant, non\-lactating female aged between 18 to 34
- •2\. Subject willing to give written informed consent
- •3\. Women of child bearing potential must have a negative urine pregnancy test
- •4\. Free of any systemic and dermatologic disorder, which in the opinion of the investigator, will interface with the study results or increase the risk of AE.
- •5\. Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.
Exclusion Criteria
- •1\. Subjects who are pregnant, breast feeding, or planning to become pregnant during the study
- •2\. Have any evidence of systematic cancer, squamous cell carcinoma, basal cell carcinoma in the last 5 years, or any other confounding skin condition.
- •3\. Have open sore or open lesions in the treatment area
- •4\. Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product.
- •5\. Have participated in any interventional clinical trial in the previous 30 days.
- •6\.Have a known sensitivity to any of the constituents of the test product including sensitivities to any of the constituents.
- •7\. Have used, are using, or are planning to use immunosuppressive or immunomodulatory medications (i.e., biologics), including corticosteroids.
- •8\. Have a history of alcohol or illegal drug/ substance abuse or suspected alcohol or illegal drug/substance abuse in the past 2 years.
Outcomes
Primary Outcomes
Not specified
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