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To study the effect and safety of facewash in men and women

Evaluation of efficacy and in use tolerance of a test product (Facewash) in men and or women. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089158
Enrollment
99
Registered
2025-06-19
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 Glo Facewash: Face will be wetted with water. Approximately 2 -3 ml of facewash will be taken on palms of hands and rubbed together to produce lather. This will be massaged on f

Sponsors

Dr. Reddys Laboratories Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary men and women between 18 and 55 years of age. 2. 32 particpants with Post Inflammatory Hyperpigmentation (any inflammation causing a blemish, for eg acne). 3. Presenting healthy skin on test sites. 4. Participant willing to provide written informed consent to participate in the study after all information concerning the study procedures and objectives has been explained. 5. Participant ready to comply with study procedures for the duration of the study

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
1. Measurement of skin pH using skin ph meter. 2. Measurement of skin hydration using MMSC 3. Evaluation of Transepidermal Water Loss using VapoMeter. 4. Measurement of skin radiance using glossmeter 5. Evaluation of pore cleansing efficacy using 3D Imaging (On 30 participants with oily skin). 6. Evaluation of skin spot/pigmentation using 3D Imaging. (On 30 participants). 7. Consumer feedback questionnaireTimepoint: Baseline, 15 mins, Day 15

Secondary

MeasureTime frame
Clinical evaluation for skin intolerancesTimepoint: 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