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Sweat resistance efficacy of the product

A CLINICAL STUDY TO EVALUATE THE SWEAT RESISTANCE EFFICACY OF TEST PRODUCT. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/060379
Enrollment
33
Registered
2023-11-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

None listed

Interventions

Intervention1: KP 57: Approximately 0.5gm of the test product is applied on randomised half face on Day 1 and Day 2 Intervention2: MD07: Approximately 0.5gm of the test product is applied on randomise

Sponsors

Hindustan Unilever Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Volunteer being able to produce at least 100 mg of sweat and whose left versus right half face sweat is more or less the same. 2. Volunteer in good health condition as per the medical screening criteria with no disease state or physical condition that the Investigator believes could interfere with the interpretation of the data. 3. Volunteer able to read, understand and sign an appropriate informed consent form indicating her willingness to participate.

Exclusion criteria

Exclusion criteria: 1. Volunteer pregnant or planning to become pregnant. 2. Volunteers who are breastfeeding or having stopped to breastfeed in the past three months. 3. Volunteers with any other signs of significant local irritation, erythema or skin disease on scalp as well as on the visible parts of the body skin site. 4. Volunteers with self-perceived sensitive skin. 5. Volunteers having chronic illness or had major surgery in the last year. 6. Volunteers undergoing any treatment of any skin condition on body.

Design outcomes

Primary

MeasureTime frame
Sweat resistance efficacyTimepoint: Day 1: 30 minutes after product application, Day 2: 30 minutes after product application

Secondary

MeasureTime frame
Sweat resistance efficacy comparison between two productsTimepoint: Day 1: 30 minutes after product application, Day 2: 30 minutes after product application

Countries

India

Contacts

Public ContactDr Mohit Lalvani

MASCOT-SPINCONTROL India Pvt. Ltd.

raji@mascotspincontrol.in02243349191

Outcome results

None listed

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