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Effect of Test Product on various skin benefit

Effect of Short term and long-term skin benefits of Ayurvedic product – A clinical study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043242
Enrollment
53
Registered
2022-06-14
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

None listed

Sponsors

Unilever Industries Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Female subjects between 25-45years of age. 2. Presence of pigment spots on face 3. Subjects with dry, oily or combination skin type. 4. Subjects who have not used fairness products or skin lightening product in past 1 month as on the screening day 5. Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the face. 6. Subject who agree not to use of any other skin lightening product/treatment/soap bar/home remedy on their face during the study period other that the study soap provided. 7. Subject who agrees not to carry out bleaching or any other skin care procedures on face during the study.

Exclusion criteria

Exclusion criteria: 1. Subjects with known skin condition that may impact the assessment 2. Subject with any other signs of significant local irritation or skin disease. 3. Subject currently taking any medication, which the Investigator believes may influence the interpretation of the data. 4. Subject having chronic illness or had major surgery in the last year. 5. Subjects undergoing any treatment of any skin condition on their face/forearm/body. 6. Subjects allergic or sensitive to bar cleansing products, creams/lotions, artificial jewelry, or anything else. 7. Subjects pregnant or nursing. 8. Subjects taking medication including food supplements.

Design outcomes

Primary

MeasureTime frame
Reduction in severity in dark spots based on visual and instrumental assessmentTimepoint: 2, 4, 8 and 12 weeks

Secondary

MeasureTime frame
Improvement in skin hydration by visual and instrumental assessmentTimepoint: 2, 4, 8 and 12 weeks

Countries

India

Contacts

Public ContactSudhanthiran S

MS Clinical Research Pvt Ltd

ritambhara@mscr.in08041125934

Outcome results

None listed

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