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To study the if the test product moisturizes and reduces itching in humans.

Evaluation of skin hydration and anti-itch properties after application of test product (Venusia Ureka cream) in men and /or women. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072479
Enrollment
32
Registered
2024-08-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

None listed

Interventions

Intervention1: Venusia Ureka Cream: Approximately 0.03 g of the product will be applied on test sites, by massaging for 30 seconds. The product will be applied once after baseline readings. Control In

Sponsors

Dr. Reddys Laboratories Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary men and /or women between 18 and 55 years of age. 2. Dry to very dry skin type (MoistureMeter SC Readings < 20). 3. Having signed a Consent Form after the study has been explained orally and in writing, of all information concerning the study procedures and study objectives. 4. Presenting healthy skin on test sites. 5. Cooperating informed of the need and duration of the examinations.

Exclusion criteria

Exclusion criteria: 1. Menopausal/Pregnant women by UPT, Lactating mothers. 2. Allergic to any cosmetic product. 3. A participant who the Investigator feels will not be compliant with study requirements. 4. Any type of skin disorder which Investigator feels will interfere with the study 5. Participants on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month). E.g. topical steroids. 6. Chronic illness which may influence the skin sensitivity (skin problems like atopic dermatitis, psoriasis, eczema or diseases like hypothyroidism, anaemia, hormonal problems, or patients on anti-cholesterol drugs, etc) 7. Any cutaneous disease which would predispose to dry skin (confirmed by prior history). 8. Any cutaneous conditions on test site (scars, moles, papules etc). 9. Subject in an exclusion period or already participating in another similar cosmetic or therapeutic trial as identified during screening on visit 1 (V1).

Design outcomes

Primary

MeasureTime frame
1. Hydration Measurement 2. TEWL measurement 3. Evaluation of itching using VAS scaleTimepoint: 0 hour, 12 hour, 24 hour, 36 hour For Vas scale- 0 hour, 6 hour anbd 12 hour

Secondary

MeasureTime frame
NoneTimepoint: Nil

Countries

India

Contacts

Public ContactDr Sagar Katare

Dr. Reddys Laboratories Ltd.

biswajitaich@drreddys.com9864159889

Outcome results

None listed

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