Study to evaluate the safety and efficacy of Skin care product for its non-comedogenic effect
- Conditions
- Health Condition 1: L708- Other acne
- Registration Number
- CTRI/2023/09/057974
- Lead Sponsor
- Kreative Beauty Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
1.Healthy Indian male/female healthy volunteers aged between 18-55 years.
2.Willing to give Informed Consent Form.
3.Mild to moderate Black heads on the face
4.Willing to complete the study assessments/questionnaires.
5.Willing to avoid usage of his/her own moisturizers and face
6.serum for at least one week before Commencement and during this study.
1.Pregnancy or breast feeding.
2.Patients with pre-existing severe systemic disease necessitating long-term medication.
3.Patients with mild to severe Anaphylaxis reactions.
4.Evidence of significant uncontrolled co-morbid disease.
5.Historyofcancer,includingsolidtumors,hematologic malignancies and carcinoma in situ
6.Any neurological (congenital or acquired), vascular or systemic disorder which could affect any of the efficacy assessments.
7.Participation in the current or previous clinical trial with any approved or investigational products during the past 1 month.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method •To assess the safety and efficacy of the product for its non-comedogenic property <br/ ><br>Following parameters will be evaluated: <br/ ><br>•Appearance of black heads <br/ ><br>•Improvementin Spotcorrection by improving the appearance of large pores <br/ ><br>Timepoint: Day 1 to Day 28
- Secondary Outcome Measures
Name Time Method To evaluate the consumer acceptance as well as their response towards the product through a feedback questionnaire.Timepoint: Day 1 to Day 28