Skip to content

To study the skin moisture after applying test products in Men and Women.

Evaluation of skin hydration after application of test product (Lotion and Cream) in men and or women. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089557
Enrollment
36
Registered
2025-06-25
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: Venusia max cream: Product application on test sites on Right volar forearms and Right upper outer arms at baseline for instrumental readings. Thereafter readings will be taken at upto

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. Having normal to dry skin, confirmed by clinical evaluation. 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. Pregnant women (confirmed orally by participants), 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).

Design outcomes

Primary

MeasureTime frame
1. Moisture evaluation for deep hydration 2. Trans epidermal water loss evaluation 3. Consumer QuestionnaireTimepoint: Baseline, 15 minutes, 12 hours, 24 hours, 48 hours, 72 hours

Secondary

MeasureTime frame
Clinical evaluation for skin intolerancesTimepoint: 12 hours, 24 hours, 48 hours, 72 hours

Countries

India

Contacts

Public ContactMs Preetha Paul

Dr Reddys Laboratories Limited

sagarkatare@drreddys.com9223772427

Outcome results

None listed

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