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SkinQ Daily Gental Cleanser for Pollution mix Dirt

An Open Label Clinick Study to evaluate the cleansing Efficacy of SkinQ Daily Gentle Cleanser for Pollution mix Dirt - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/100849
Enrollment
32
Registered
2026-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

None listed

Interventions

Intervention1: Test Product: SkinQ Daily Gental Cleanser: Test Product: SkinQ Daily Gentle cleanser, Apply polution mix dirt on face evenly wait till it settle down on face. Route of administration: T

Sponsors

Health Q Life Sciences Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Gender: Male or Female 18 to 45 2) Subjects willing to give written informed consent. 3) Volunteers with Normal to dry skin 4) Women of child bearing potential must have a negative urine pregnancy test prior to study entry. 5) 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. 6) 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. Use of systemic acne medications (e.g., oral isotretinoin within past 6 months) or topical prescription acne medications within 4 weeks. 2. Significant dermatologic conditions other than acne that could interfere with assessments. 3. Known sensitivity to product ingredients. 4. Recent facial procedures (chemical peels, lasers) within 4 weeks. 5. Have participated in any interventional clinical trial in the previous 90 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 not skin related issues.

Design outcomes

Primary

MeasureTime frame
Change in pH Change in TEWL Dermascope imagingTimepoint: T0min, T+15 mins

Secondary

MeasureTime frame
Not ApplicableTimepoint: Not Applicable

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org08937015757

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026