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TO ESTIMATE THE EFFECTIVENESS AND TOLERANCE OF A SKIN ANTI AGEING TEST PRODUCT IN WOMEN

EVALUATION OF THE EFFICACY AND TOLERANCE OF A SKIN ANTI AGEING TEST PRODUCT IN WOMEN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/11/002099
Enrollment
26
Registered
2011-11-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Coenzyme Q10 Topical Gel (1 mg/gm).: Gently apply 2 FTU of the product (1.0 g) to cleansed face & neck twice a day. Massage in an upward motion until fully absorbed.Product will be appl

Sponsors

Inventia Healthcare Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary women with moderate wrinkles (not greater than 2- 3 fine lines extending upto lateral end of eyebrow, but not beyond). 2. Age Limit: 35 â?? 55 years. 3. Has been fully informed verbally and in writing and comply with the study specifications. Signature for participation in test. 4. Photo type: III (White skin which sometimes burns, difficult to tan) and IV (Moderate brown skin which rarely burns and tans with ease). 5. Accepting not to use products with same end benefit, or containing sunscreen, during the study. 6. Co-operating, informed of the need and duration of the examinations. 7. For which the Investigator considers that the compliance will be correct.

Exclusion criteria

Exclusion criteria: 1. Skin allergy antecedents or atopic subject. 2. Pregnant women (as confirmed by UPT) and lactating women. 3. Seasonal allergies/Hyper sensitivity to any cosmetic product. 4. Any clinically significant systemic or cutaneous disease, which may interfere with study treatments or procedure. 5. Subjects on any medical treatment either systemic/topical in the past 1 month which may interfere with the performance of the study treatment. 6. Subject in an exclusion period or participating in any other similar cosmetic or therapeutic trial as identified during screening on visit 1 (V1).

Design outcomes

Primary

MeasureTime frame
The Primary Evaluation criteria (Primary Objective) for this study: â?¢ Measuring depth of wrinkles around crowâ??s feet area using PRIMOS â?¢ Hydration of Stratum corneum by MoistureMeter SC â?¢ Cutometer measurements for elasticity and firmness. The Secondary Evaluation Criteria (Primary Objective) for this study: â?¢ Self evaluation questionnaire to evaluate the product efficacy and sensorial properties. â?¢ Clinical Evaluation using skin age score. Timepoint: The Primary Evaluation criteria (Primary Objective) : â?¢ Measuring depth of wrinkles using PRIMOS on Day 0 and Day 30. â?¢ Hydration by MoistureMeter SC on Day 0, 15 and 30. â?¢ Cutometer measurements for elasticity and firmness on Day 0, 15 and 30. The Secondary Evaluation Criteria (Primary Objective) : â?¢ Self evaluation questionnaire to evaluate the product efficacy and sensorial properties on Day 15 and 30. â?¢ Clinical Evaluation using skin age score on Day 0, 15 and 30.

Secondary

MeasureTime frame
â?¢ Clinical Evaluation for toleranceTimepoint: Day 15 and Day 30

Countries

India

Contacts

Public ContactDr Ganeshchandra Sonavane
rsjdr@rediffmail.com66758851

Outcome results

None listed

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