A study to check the Cleansing effects.

Not Applicable

Completed

• Registration Number: CTRI/2023/02/049445
• Lead Sponsor: HNL Business Services India Private Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-03-15
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 35

Inclusion Criteria

1. Male and female adult subjects in general good health as determined from

a recent medical history.

2. Subjects belonging to one of the skin types ie dry, normal, oily or

combination normal, dry skin type.

3. Subjects should refrain from washing their face for 12 hrs prior to test

product application.

4. Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds,

lacerations, or any other active skin conditions on the face.

5. Subject to agree to remove all jewellery etc. during assessments.

6. Subjects willing to give a voluntary written informed consent and agree to

come for regular follow up.

7. Subjects willing to abide by and comply with the study protocol.

8. Subjects who have not participated in a similar investigation in past four

weeks.

9. Subjects who are willing not to participate in any other clinical study during

participation in the current study.

Exclusion Criteria

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

2. Subject currently taking any medication, which the investigator believes may influence the interpretation of the data.

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

4. Subjects undergoing any treatment of any skin condition.

5. Subjects not willing to discontinue other topical skin care products until completion of the study.

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

7. Subjects with any underlying uncontrolled medical illness including diabetes mellitus, hypertension, liver disease or history of alcoholism, HIV, hepatitis,

or any other serious medical illness.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Significant improvement in skin cleansing <br/ ><br>2. Significant improvement in shine/oil control <br/ ><br>3. Significant improvement in greasiness <br/ ><br>Timepoint: Before and After use

Secondary Outcome Measures

Name	Time	Method
oneTimepoint: NA