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1% Hyaluronic Sunscreen Aqua Gel for plumper-looking skin, and reduction in skin dryness

An open-label clinical study to check the efficacy of 1% Hyaluronic Sunscreen Aqua Gel on hydration, plumper-looking skin, and reduction in skin dryness in healthy volunteers - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/09/094638
Enrollment
36
Registered
2025-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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: 1% Hyaluronic Sunscreen Aqua Gel: Route of administration: Topical, Frequency :gently apply 1gm of the gel and massage in outward direction, Duration: 1day Control Inter

Sponsors

THE DERMA CO.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Gender: Non-pregnant, non-lactating female Age 18?55 years. 2. Subject willing to give written informed consent 3. Women of child bearing potential must have a negative urine pregnancy test 4. Fitzpatrick skin type II?V. 5. Healthy skin on test areas. 6. Agree to avoid other facial actives 7 days prior to visit.

Exclusion criteria

Exclusion criteria: 1. Subjects who are pregnant, breast feeding, or planning to become pregnant during the study 2. Have any evidence of systematic cancer, squamous cell carcinoma, basal cell carcinoma in the last 5 years, or any other confounding skin condition. 3. Have open sore or open lesions in the treatment area 4. Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product. 5. Have participated in any interventional clinical trial in the previous 30 days. Known allergy to product ingredients. 6. Active dermatitis, wounds or lesions on test areas. 7. Facial procedures in prior 4 weeks (e.g., peels, lasers). 8. Systemic retinoids in prior 6 months.

Design outcomes

Primary

MeasureTime frame
1. change in skin hydration 2. DSLR Imaging 3. Dermatologist visual grading Timepoint: At T0, 30 minutes, 2 hour and 8 hours

Secondary

MeasureTime frame
1. SGATimepoint: At T0, 30 minutes, 2 hour and 8 hours

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org08937015757

Outcome results

None listed

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