Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00711256
Other study ID # H-B-2007-120
Secondary ID
Status Recruiting
Phase N/A
First received July 7, 2008
Last updated July 7, 2008
Start date July 2008
Est. completion date November 2008

Study information

Verified date April 2008
Source Bispebjerg Hospital
Contact Hans Christian Wulf, Dr.med
Phone +45 3135 3155
Is FDA regulated No
Health authority Denmark: Danish Dataprotection AgencyDenmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

The investigators want to investigate whether sunscreen is removed by clothing and to what extend when the amount of sunscreen applied varies.Does clothing reduce the SPF when clothes are put on 20, 8, or 4 minutes after sunscreen application? The investigators also want to investigate the persistence of sunscreen during eight hours indoor. How much does the SPF reduces? Furthermore, we want to investigate whether sunscreen in the layers 2, 1, and 0.5 mg/cm2 reduce the vitamin D production in the skin.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date November 2008
Est. primary completion date August 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Healthy participants.

- > 18 years.

- Skin type I, II, and III.

Exclusion Criteria:

- Pregnancy.

- Medicin use.

- Skin or other diseases.

- The participants must not have been in solarium or gotten sun on their trunks in the 3 months before the study start and during the study.

- Skin types IV and above.

Study Design

Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Other:
sunscreen MATAS sunlotion SPF 8

Radiation:
UVB light
duration 4 times 1 minute radiation on the trunk.

Locations

Country Name City State
Denmark Bispebjerg Hospital Copenhagen Kbh Nv

Sponsors (1)

Lead Sponsor Collaborator
Bispebjerg Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary vitamin D (nmol) meassured in a blood sample. 5 days after sunscreen use and UV light exposure No
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT04618536 - Comparison of Sun Protection Factor 30 Persistence Between Inorganic and Organic Sunscreen in Swimmer N/A