Skin Benefit Study For The Test Product

Not Applicable

Completed

• Registration Number: CTRI/2021/07/034591
• Lead Sponsor: nilever Industries Pvt Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-10-25
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 508

Inclusion Criteria

1.Male and female subjects between 18 to 45 years of age. (both age inclusive).

2.Healthy male and female subjects as per their medical history and medical examination.

3.Subjects with normal, oily or combination in skin type.

4.Subjects with common skin ailments.

5.Subjects who have not used fairness products in past 1 month as on the screening day.

6.Subject who agree not to use of any other products on their face during the study period.

7.Subject to agree not to carry out bleaching or any other skin care procedures on face during the study period.

8.Subject to agree to remove all jewellery on/around face (e.g., necklace, earrings, if possible, nose ring) during imaging.

Exclusion Criteria

1.Subjects presenting any skin ailment that may require medical intervention as per the investigatorââ?¬•s discretion.

2.Subjects with known skin condition that may impact the assessment.

3.Subject with any other signs of significant local irritation or skin disease.

4.Subject currently taking any medication, which the Investigator believes may influence the interpretation of the data.

5.Subject having chronic illness or had major surgery in the last year.

6.Subjects with dry to very dry skin, which will interfere with the test assessments.

7.Subjects undergoing any treatment of any skin condition on their face/forearm/body.

8.Subject allergic or sensitive to bar cleansing products, creams/lotions, artificial jewellery or anything else.

9.Subject pregnant or nursing.

10.Subjects taking medication including food supplements.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Significant improvement in skin conditions by Expert assessmentTimepoint: Baseline, 2 weeks, 4 weeks & 6 weeks

Secondary Outcome Measures

Name	Time	Method
Significant improvement in skin conditions by instrumental assessmentTimepoint: Baseline, 2 weeks, 4 weeks & 6 weeks