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To study the reduction in pimples.

A study to evaluate the reduction of acne.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043346
Enrollment
12
Registered
2022-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

None listed

Interventions

Intervention1: Clincitop gel: Usage Instructions: Wash face with a facewash. Apply a small amount of the product on acne affected area only. Repeat twice a day-Morning and night for 14 days. Control

Sponsors

CLAIMS PVTLTD
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary men/women with mild to moderate inflammatory acne between 18 years 40 years. 2. No treatment for acne in the past 1 month 3. Accepting not to use products with the same end benefit during the entire study duration. 4. For whom the Investigator considers that the compliance will be correct. 5. Cooperating, informed of the need and duration of the examinations, and ready to comply with protocol procedures. 6. Having signed a Consent Form and will be once informed orally and in writing of all information concerning the study procedures and study objectives.

Exclusion criteria

Exclusion criteria: 1. Pregnant women (by UPT) and lactating women. 2. History suggestive of any hormonal problems. 3. History of allergic dermatitis or contact allergy to cosmetics, 4. Hypersensitivity to any cosmetic product, 5. Any clinically significant systemic or cutaneous disease, which may interfere with study treatments or procedures. 6. 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). 7. Participant in an exclusion period or participating in another similar cosmetic or therapeutic trial.

Design outcomes

Primary

MeasureTime frame
To evaluate reduction in acne post treatment in 2 groups given different treatments from baseline. Timepoint: Day 0, Day 15

Secondary

MeasureTime frame
To compare of the reduction in acne post treatment in 2 groups given different treatments. Timepoint: Day 0, Day 15

Countries

India

Contacts

Public ContactShaziya Sajun Merchant

C.L.A.I.M.S. PVT.LTD

rsjdrs@gmail.com66758851

Outcome results

None listed

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