Skip to content

Prospective study to evaluate the safety of transdermal absorption of different sunscreens by human using

Prospective study to evaluate the safety of transdermal absorption of different sunscreens by human using

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078046
Enrollment
Unknown
Registered
2023-11-28
Start date
2023-11-28
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

skin permeability

Interventions

Sunscreen 1:Apply the Sunscreen 1
Sunscreen 2:Apply the Sunscreen 2

Sponsors

Huashan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Healthy adult men and women aged 18-60; 2. Have not used products containing sunscreen in two weeks, including sunscreens, creams, lotions and BB cream with SPF; 3. Willing to participate in the experiment, and able to complete the skin test as required during the whole research process; 4. Have read and signed the informed consent before the study begins; 5. In good health at the time of the test; 6. BMI is 18.5-29.9; 7. No planned pregnancy within 1 month before and after the test; 8. Subjects self-reported non-sensitive skin; 9. Can complete the prescribed content according to the requirements of the test plan.

Exclusion criteria

Exclusion criteria: 1. Patients with serious systemic disease who are currently using systemic or local topical corticosteroids, retinoic acid, vasoconstrictors, antibiotics, anti-inflammatory drugs, etc., or within one month before the start of this study; 2. Patients with severe allergic diseases or who have had cosmetic allergies in the last 1-2 years; 3. Allergic history of daily use of sunscreen products; 4. Pregnant, breastfeeding or planning to become pregnant; 5. Oral contraceptives (nearly 3 months and throughout the study period); 6. Allergic to alcohol; 7. The test area has a large area of acne, tattoos and other skin conditions that affect the test results; 8. There is A history of skin or other medical conditions that affect the results of the test and other conditions that prevent the use of the test sample; 9. Have participated in other clinical trials at present or within 3 months before the start of this study; 10. There are other conditions that the investigator deems unsuitable for participation in the trial.

Design outcomes

Primary

MeasureTime frame
Sunscreen content in Blood;

Secondary

MeasureTime frame
Safety Evaluation;

Countries

China

Contacts

Public ContactLeihong Xiang

Huashan Hospital

flora_xiang@vip.163.com+86 138 1825 2671

Outcome results

None listed

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