The Sun Protection Effect and Efficacy in Treatment of Sunburn Using Topical Corticosteroids.
Primary Purpose
Sunburn
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
corticosteroids
Sponsored by
About this trial
This is an interventional treatment trial for Sunburn focused on measuring sunburn, corticosteroids
Eligibility Criteria
Inclusion Criteria: 18 years or older, healthy, fair skinned (skin type I-III) Exclusion Criteria: Pregnant or lactating women.In treatment with corticosteroids.
Sites / Locations
- Bispebjerg HospitalRecruiting
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00206882
First Posted
September 12, 2005
Last Updated
October 10, 2006
Sponsor
Bispebjerg Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00206882
Brief Title
The Sun Protection Effect and Efficacy in Treatment of Sunburn Using Topical Corticosteroids.
Study Type
Interventional
2. Study Status
Record Verification Date
August 2005
Overall Recruitment Status
Unknown status
Study Start Date
September 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Bispebjerg Hospital
4. Oversight
5. Study Description
Brief Summary
The purpose of the study is to evaluate the sun protection effect and efficacy in treatment of sunburn using topical corticosteroids in a randomised controlled and investigator blinded trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sunburn
Keywords
sunburn, corticosteroids
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Double
Allocation
Randomized
Enrollment
20 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
corticosteroids
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18 years or older, healthy, fair skinned (skin type I-III)
Exclusion Criteria:
Pregnant or lactating women.In treatment with corticosteroids.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hans Christian Wulf, M.D., Dr. Sc.
Phone
+45 35 31 31 55
Email
HCW01@bbh.hosp.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans Christian Wulf, M.D., Dr.Sc.
Organizational Affiliation
Bispebjerg Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Bispebjerg Hospital
City
Copenhagen
State/Province
Copenhagen NV
ZIP/Postal Code
2400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hans Christian Wulf, M.D., Dr.Sc.
Phone
+45 35 31 31 55
Email
HCW01@bbh.hosp.dk
12. IPD Sharing Statement
Citations:
PubMed Identifier
18490588
Citation
Faurschou A, Wulf HC. Topical corticosteroids in the treatment of acute sunburn: a randomized, double-blind clinical trial. Arch Dermatol. 2008 May;144(5):620-4. doi: 10.1001/archderm.144.5.620.
Results Reference
derived
Learn more about this trial
The Sun Protection Effect and Efficacy in Treatment of Sunburn Using Topical Corticosteroids.
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