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To study the effect and safety of a Neck cream in men and women.

Evaluation of the efficacy of a Neck Repair Night Cream in men and women and its in use tolerance. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106662
Enrollment
27
Registered
2026-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

None listed

Interventions

Intervention1: Neck Night Repair Cream: Neck will be washed and dabbed dry with towel. A thin layer of Neck Skin Cream (approximately 1g) will be applied on neck, by gentle rubbing, 3 times a week at

Sponsors

Earthy Biome Pvt. Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary men and/or women from 40 years to 60 years of age. 2. Volunteers with lines/loose skin on neck. 3. Having apparently healthy skin on test area. 4. Willingness to discontinue the use of other cosmetic products on neck skin during the course of the study. 5. Willing to avoid unusual sun exposure as far as possible for the entire study duration. 6. Accepting not to use products with the same end benefit during the entire study duration. 7. Cooperating, informed of the need and duration of the examinations, and ready to comply with protocol procedures. 8. Ready to provide consent, having been informed orally and in writing of all information concerning the study procedures and study objectives.

Exclusion criteria

Exclusion criteria: 1. Female who is pregnant by UPT or lactating. 2. Participants hypersensitive to any of the component of the test product. 3. Participants having any hard damage to skin (e.g., excessive sunburn or suntan). 4. Participants on any systemic medical treatment which may interfere with the performance of the study treatment (presently or in the past 1 month). 5. Participant in an exclusion period or participating in any clinical trial within 30 days prior to screening.

Design outcomes

Primary

MeasureTime frame
1. 3D Imaging on neck area. 2. Skin elasticity using CutoMeter. 3. Self-assessment for product efficacy.Timepoint: Day 0, Day 30, Day 60—

Secondary

MeasureTime frame
1. Clinical evaluation for in use tolerance. 2. Self-assessment questionnaire for in use tolerance.Timepoint: Day 0, Day 30, Day 60—

Countries

India

Contacts

Public ContactMs Preetha Paul

Clinical Aesthetics and Investigative Management Service Pvt. Ltd. (C.L.A.I.M.S.PVT.LTD.

preetha@claimsclinical.com66758851

Outcome results

None listed

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