To study the effectiveness of a test product on volunteers with acne scars
- Registration Number
- CTRI/2022/01/039598
- Lead Sponsor
- Amvigor Organics Pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 34
1. Voluntary men and/or women in the age group of 18 to 45 years.
2. Volunteers with acne scars
3. Patients without any scar treatment done in the past 6 months.
4. Having signed a Consent Form after being informed orally and in writing of all information
concerning the study procedures and study objectives.
5. Ready to comply with the study specifications.
6. Willing to refrain from use of all other topical medications that would affect the results of the trial.
7.No history of allergic dermatitis or contact allergy to cosmetics.
1. Pregnant women confirmed by UPT , Lactating mothers.
2. Participants with hypertropic acne scars.
3. Known sensitivity to any of the ingredients in the study product.
4. Presence of other skin conditions, diseases, or medical conditions that (per protocol or in
the opinion of the Investigator) may require concurrent therapy, interfere with the
evaluation of the study medication, or compromise participant safety.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Change in depth of acne scars using 3D Imaging. <br/ ><br>2. Clinical Photography to observe the change in depth of acne scars <br/ ><br>3. Subject self evaluation questionnaireTimepoint: Day 0, Day 28, Day 56
- Secondary Outcome Measures
Name Time Method To evaluate the in-use tolerance of the Product via clinical evaluation and self assessment questionnaireTimepoint: Day 0, Day 28, Day 56