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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
Bispebjerg Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sunburn focused on measuring sunburn, corticosteroids

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

First Posted
September 12, 2005
Last Updated
October 10, 2006
Sponsor
Bispebjerg Hospital
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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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