Affect of Dose Rate on UVR Induced Skin Erythema

Status Not yet recruiting

Clinical Trial Summary

Purpose of study: Evaluation of the affect of dose rate on UVR induced skin erythema.

Study design: A single-center, prospective, randomized, crossover, open study.

Number of patients: 20-40

Patient population: Healthy volunteers

Control: Different sites on patients body

Procedure duration: Total 3-5 hours (4 visits)

Duration of follow up: 4 days

Duration of study: Up to 6 months

Primary objectives: To examine the difference in erythemal response as a function of dose rate, and to assess the total amount of energy that is theoretically transmitted through a sunscreen within the range of SPF 2-10.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

Erythema

Clinical Trial Details

NCT number	NCT00785187
Study type	Interventional
Source	Goldenhersh, Michael, M.D.
Contact
Status	Not yet recruiting
Phase	N/A
Start date	December 2008

View Details

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