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To study the effect of serum in reducing pimples and making the skin look younger in Women.

A monocentric, single group, 4 week trial to evaluate the efficacy of a serum in inflammatory acne and skin anti ageing and in use tolerance of the serum. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089685
Enrollment
34
Registered
2025-06-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

None listed

Interventions

Intervention1: BLEMISH BALANCE SERUM: Face will be washed and dabbed dry with towel. A thin layer of the Face Serum (approximately 0.5 ml) will be applied on the face, once at night for a duration of

Sponsors

Earthy Biome Pvt. Ltd. 14
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary women from 30 years to 55 years of age. 2. Participants with inflammatory acne, Blemish, Sunspots, PIH. 3. 10 participants with blemish (at least 1 hyperpigmented spot like PIH) 4. 10 Participants with mild to moderate wrinkles in crowâ??s feet area. 5. Having apparently healthy skin on test area. 6. Willingness to discontinue the use of other cosmetic products on face during the course of the study. 7. Willing to avoid unusual sun exposure as far as possible for the entire study duration. 8. Accepting not to use products with the same end benefit during the entire study duration. 9. Cooperating, informed of the need and duration of the examinations, and ready to comply with protocol procedures. 10. 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 women. 2. Participants having any hard damage to skin (e.g., excessive sunburn or suntan). 3. Participants hypersensitive to any of the components of the test product. 4. Participants on any systemic medical treatment which may interfere with the performance of the study treatment (presently or in the past 1 month).

Design outcomes

Primary

MeasureTime frame
1. 3D Imaging for acne, wrinkles, skin texture, blemish and pore cleansing efficacy. 2. Clinical grading for inflammatory acne count. 3. Self-assessment for product efficacy.Timepoint: Day 0, Day 30—

Secondary

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

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: Jun 29, 2026