None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 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.
Exclusion criteria
Exclusion criteria: 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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Change in depth of acne scars using 3D Imaging. 2. Clinical Photography to observe the change in depth of acne scars 3. Subject self evaluation questionnaireTimepoint: Day 0, Day 28, Day 56 | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the in-use tolerance of the Product via clinical evaluation and self assessment questionnaireTimepoint: Day 0, Day 28, Day 56 | — |
Countries
India
Contacts
AMVIGOR ORGANICS PVT. LTD