MedPath

To evaluate the efficacy of test products in PreventingAcne Flare ups and Associated Symptoms in Healthy Human Volunteers

Phase 2
Completed
Registration Number
CTRI/2018/04/013491
Lead Sponsor
ITC Life Sciences Technology Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
80
Inclusion Criteria

1.Volunteer in the age group of 18 to 35 years

2.Atleast 70 subjects with Oily / Acne prone skin

3.Atleast 10 subjects with Acne eruptions on the back

4.Atleast 10 subjects with Dry skin + Acne on face

5.Volunteer willing to participate in the study and provide signed informed consent for the same.

6.Volunteer willing to abide by the study protocol and refrain from using any product other than the provided Investigational product during the study course.

7.Volunteers willing to visit the site for periodic assessments on the scheduled dates.

8.Volunteer who exhibits good tolerance to the investigational product with no signs of sensitivity.

Exclusion Criteria

1.Pregnant or lactating women

2.Volunteer undergoing treatment for anti-acne or skin lightening

3.Volunteer with pre-existing systemic disease requiring long-term medication as disclosed by volunteers

4.Volunteer with genetic and endocrinal disorders as disclosed by volunteers

5.Volunteer with drug induced acne as disclosed by volunteers

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath