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study evaluating oil control benefit from using a face wash

A clinical study to evaluate the cleansing efficacy of a face wash in providing oil control benefits to healthy subjects.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053661
Enrollment
40
Registered
2023-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Men Intense Oil Clear Lemon face wash. (Batch Number:B7723000650: Post splashing of the whole face with water, a small quantity of the test product will be taken on to the palm of the s

Sponsors

Himalaya Wellness Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: For Group 1: 1. Sufficient number of male subjects will be enrolled and 40 are required to complete the study. 2. Male adult subjects in general good health as determined from a recent medical history. For Group 2: 1. Sufficient number of male and female subjects (1:3) will be enrolled and 40 are required to complete the study. 2. Male and female adult subjects in general good health as determined from a recent medical history. Common for both group: 1. Subjects with oily skin with sebum =130 2. Subjects should refrain from washing their face for 12 hrs prior to test product application. 3. Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the face. 4. Subject to agree to remove all jewellery etc. during assessments. 5. Subjects willing to give a voluntary written informed consent and agree to come for regular follow up. 6. Subjects willing to abide by and comply with the study protocol. 7. Subjects who have not participated in a similar investigation in past four weeks. 8. Subjects who are willing not to participate in any other clinical study during participation in the current study.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
1. To evaluate the efficacy of the test products immediately, at 4hrs, 8hrs & 12hrs & also at day 8 as per below parameters when compared to baseline and water control i.Skin cleansing ii.Shine/oil control iii.Greasiness 2. To evaluate the efficacy of test product in providing oil control for X hours in comparison to the baseline and water control.Timepoint: T-immdediate, 4hr, 8hr, 12 hr & day 8.

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactDr Mukesh Ramnane

MS Clinical Research Pvt Ltd

mukesh.ramnane@msclinical.com08041125934

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026