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The Sun Protection Effect and Efficacy in Treatment of Sunburn Using Topical Corticosteroids.

NCT ID: NCT00206882

Last Updated: 2006-10-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Sunburn

Keywords

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sunburn corticosteroids

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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corticosteroids

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* 18 years or older, healthy, fair skinned (skin type I-III)

Exclusion Criteria

* Pregnant or lactating women.In treatment with corticosteroids.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Bispebjerg Hospital

OTHER

Sponsor Role lead

Principal Investigators

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Hans Christian Wulf, M.D., Dr.Sc.

Role: STUDY_DIRECTOR

Bispebjerg Hospital

Locations

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Bispebjerg Hospital

Copenhagen, Copenhagen NV, Denmark

Site Status RECRUITING

Countries

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Denmark

Central Contacts

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Hans Christian Wulf, M.D., Dr. Sc.

Role: CONTACT

Phone: +45 35 31 31 55

Email: [email protected]

Facility Contacts

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Hans Christian Wulf, M.D., Dr.Sc.

Role: primary

References

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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.

Reference Type DERIVED
PMID: 18490588 (View on PubMed)

Other Identifiers

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KF-01-272662

Identifier Type: -

Identifier Source: org_study_id