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Multiple use test to evaluate the skin benefits of ayurvedic products

Efficacy Evaluation of Ayurvedic products ââ?¬â?? a short term study - None

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035784
Enrollment
55
Registered
2021-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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.Healthy male and female subjects between 18-45 years of age. 2.Subjects with dry skin as per instrument assessment 3.Subjects with sufficiently long and broad forearms to accommodate the test sites 4.Subjects with uniform skin tone on volar forearm 5.Subjects who have not participated in any clinical product evaluation test in the past 1 month 6.Subjects willing to give a voluntary written informed consent for activities in the study for imaging and agree to come for regular study visits 7.Subjects willing to abide and comply with the study protocol 8.Subjects who are willing not to participate in any other clinical study during participation in the current study. 9.Subjects free of excessive hair, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the forearm. 10.Subjects who agree not to use of any other product/treatment/soap bar on their forearm during the study period other than product provided 11.Subjects who agree not to carry out bleaching or any other procedures on forearm during the study period.

Exclusion criteria

Exclusion criteria: 1.A known history or present condition of allergic response to any sunscreen products, cosmetics products, bathing soaps, detergent powder or medicine 2.Subjects with visible photo-damage on their forearms 3.Subjects having active skin diseases which will interfere with assessments 4.Subjects on oral and topical medications which will compromise the study. 5.Suffering from autoimmune diseases like thyroid autoimmunity or diabetes mellitus. 6.Subjects who are pregnant, lactating or nursing

Design outcomes

Primary

MeasureTime frame
Dermatologist assessment on different skin parametersTimepoint: Baseline and Post treatment

Secondary

MeasureTime frame
Instrument assessment of different skin parametersTimepoint: Baseline and Post treatment

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