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Residual assessment of active ingredients of sunscreen products in human blood

Residual assessment of active ingredients of sunscreen products in human blood

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103219
Enrollment
Unknown
Registered
2025-05-27
Start date
2024-09-14
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Sunscreen product blood residue

Interventions

Sunscreen product 1:Apply the appropriate sunscreen product
Sunscreen product 2:Apply the appropriate sunscreen product
Sunscreen product 3:Apply the appropriate sunscreen product
Sunscreen product 4:Apply the appropriate sunscreen product

Sponsors

The University of Hong Kong-Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary participation in the project. 2. Volunteers aged 18-60 years old with the habit of using sunscreen products; 3. Healthy skin, no skin diseases and other factors affecting the test. 4. No use of other sunscreen products for 1 week; 5. No history of allergy to cosmetics and other topical sunscreen products.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women. 2. Use of antihistamines in the past week or immunosuppressants in the past month; 3. The presence of scar, pigment, atrophy, port wine stain or other skin diseases in the test area of the skin, which may affect the test results. 4. Patients with serious diseases. 5. Systemic and topical use of any drugs that affect skin color during the trial. 6. Those who are allergic to the test product.

Design outcomes

Primary

MeasureTime frame
Zinc oxide;Titania;Ethylhexyl Methoxycinnamate;Ethylhexyl salicylate;

Countries

China

Contacts

Public ContactLi Hao

The University of Hong Kong-Shenzhen Hospital

lihao@hku-szh.org+86 186 4026 2823

Outcome results

None listed

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