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To study the efficacy of Retinol Serum for skin Brightening

A Clinical Study to evaluate the efficacy of skin Renew Peptide Retinol Serum for skin Brightening - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066514
Enrollment
36
Registered
2024-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

None listed

Interventions

Intervention1: Skin Renew Peptide Retinol Serum: Test Product: Skin Renew Peptide Retinol Serum Dose: gently massage approx. 8 drops serum over the face with fingers in outward manner two times a day.

Sponsors

Honasa Consumer Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Gender: Non-pregnant, non-lactating female aged between 25 to 45. 2) Subjects willing to give written informed consent 3) Women of childbearing potential must have a negative urine pregnancy test prior to study entry. 4) Are free of any systemic or dermatologic disorder, which, in the opinion of the investigator, will interfere with the study results or increase the risk of adverse events. 5) Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.

Exclusion criteria

Exclusion criteria: 1. Subjects who are pregnant, breast-feeding, or planning to become pregnant during the study. 2. Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition. 3. Have open sores or open lesions in the treatment area(s). 4. Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product. 5. Have participated in any interventional clinical trial in the previous 30 days. 6. Have a known sensitivity to any of the constituents of the test product. 7. Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including corticosteroids. 8. Have a history of alcohol or illegal drug or substance abuse, or suspected alcohol or illegal drug or substance abuse in the past 2 years.

Design outcomes

Primary

MeasureTime frame
change in dark spot reduction, an evens out tone, Skin elasticity and firmness pigmentation and hyperpigmentationTimepoint: Day 0, Day 14 and Day 28

Secondary

MeasureTime frame
To assess the safety and tolerabilityTimepoint: Day 0, Day 14 and Day 28

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org8937015757

Outcome results

None listed

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