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To study the safety and likeability of Sunscreen in men and or women.

Evaluation of sensorial properties and in use tolerance of Test Product (Sunscreen) in men and or women. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088519
Enrollment
55
Registered
2025-06-10
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 Invisible Sunscreen: Approximately 0.5 gm of sunscreen will be taken and applied on face and massaged gently. Product will be used daily, for 15 days, half an hour before going

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 signed a Consent Form after the study has been explained orally and in writing, of all information concerning the study procedures and study objectives. 3. Presenting healthy skin on test sites. 4. Cooperating informed of the need and duration of the examinations.

Exclusion criteria

Exclusion criteria: 1. 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.

Design outcomes

Primary

MeasureTime frame
Consumer feedback questionnaire Timepoint: Day 15

Secondary

MeasureTime frame
Clinical evaluation for skin intolerances.Timepoint: Day 15

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