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Effect of face cleansing in improving skin conditions

A clinical study to assess the efficacy of test products in improving biophysical properties of skin upon face cleansing. - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096537
Enrollment
96
Registered
2025-10-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

None listed

Interventions

Intervention1: DF21: The product is applied on the face, gently lathered for 15 seconds, and rinsed off with water. The face is then patted dry. The total duration of application is 3 days Interventio

Sponsors

Hindustan Unilever Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Healthy female volunteers 2)Volunteers with dull skin 3)Volunteers with dark spots 4)Volunteer in good health condition as per the medical screening criteria 5)Volunteer able to read, understand and sign an appropriate informed consent form indicating her willingness to participate. 6)Volunteers agreeing to comply with following study restrictions: 7)Willing to refrain from application of any other product/treatment on their face during wash off and treatment phase 8)Not to apply any cosmetic, skin care product or home remedies or any other face cleanser/wash/soap etc at home during the study period

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 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 having chronic illness or had major surgery in the last year. 5)Volunteers undergoing any treatment of any skin condition on body. 6)Volunteers known to have allergies to cosmetics 7)Volunteers taking any food supplements

Design outcomes

Primary

MeasureTime frame
Improvement in Brightness, Hydration Timepoint: Baseline, Day 1, Day 2, Day 3

Secondary

MeasureTime frame
Safety assessments like redness and drynessTimepoint: Baseline, Day 1, Day 2, Day 3

Countries

India

Contacts

Public ContactDr Mohit Lalvani

MASCOT-SPINCONTROL India Pvt. Ltd.

niharika@mascotspincontrol.in02243349191

Outcome results

None listed

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