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To study benefits of facewash on pimples in men and women.

Evaluation of efficacy and in use tolerance of Test Product (Acne Facewash) in men and or women. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089480
Enrollment
77
Registered
2025-06-24
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 Acne 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. Men and women with age of greater than or equal to 15 years. 2. 30 Participants with Acne grade 2-3 skin type, according to IGA scale. 3. Presenting healthy skin on test sites. 4. Participant willing to voluntarily 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 protocol procedures for the duration of the study.

Exclusion criteria

Exclusion criteria: 1. Women with confirmed pregnancy through a urine pregnancy test (UPT) and / or Lactating mothers. 2. Participants who are allergic to any cosmetic product. 3. Participant who the Investigator feels will not be compliant with study requirements. 4. Participants with any type of skin disorder 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 at baseline, before and 15-20 minutes after washing face with facewash and after 15 days of usage. 2. Evaluation of Transepidermal Water Loss using VapoMeter at baseline and Day 15. 3. Evaluation of pore cleansing efficacy using 3D Imaging (On 30 participants with oily skin) before and after washing face with facewash on Day 0 and Day 15. 4. Analysis of single acne using 3D Imaging at baseline and Day 15. 5. Clinical grading for acne at baseline and Day 15 6. Consumer feedback questionnaireTimepoint: Day 0, Day 15

Secondary

MeasureTime frame
Clinical evaluation for in use tolerance using following scale.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