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Clinical Evaluation of Bacitracin

Primary Purpose

Allergic Contact Dermatitis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
bacitracin (allergen)
Sponsored by
Mekos Laboratories AS
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Allergic Contact Dermatitis focused on measuring Allergic contact dermatitis, Patch testing, bacitracin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Positive bacitracin patch test within the latest 5 years. Age greater than or equal to 18 years. Signed informed consent. Exclusion Criteria: Topical treatment with corticosteroids or immunosuppressives during the latest 7 days on the test area or near the test area. Systemic treatment with corticosteroids or immunosuppressives during the latest 7 days. Treatment with ultraviolet (UV)-light during the latest 3 weeks. Widespread active dermatitis or dermatitis on test area. Breast-feeding or pregnancy. Females of childbearing potential must demonstrate a negative pregnancy test before inclusion in the study. Subjects not able to cooperate.

Sites / Locations

  • Dermatological Clinic (Joseph Fowler MD)

Outcomes

Primary Outcome Measures

Skin reaction to the patch test after 72-96 hours and after 7 days

Secondary Outcome Measures

Evaluation of safety including late and persistent responses
Evaluation day 3/4, day 7 and day 21

Full Information

First Posted
August 19, 2005
Last Updated
October 18, 2005
Sponsor
Mekos Laboratories AS
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1. Study Identification

Unique Protocol Identification Number
NCT00132600
Brief Title
Clinical Evaluation of Bacitracin
Official Title
Clinical Evaluation of Bacitracin. A Phase II Dose-Response Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
April 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Mekos Laboratories AS

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to establish a concentration of a bacitracin-patch for diagnosing allergic contact dermatitis.
Detailed Description
Thin-layer Rapid Use Epicutaneous Test (T.R.U.E. Test®) is a ready-to-use patch test method designed for diagnosis of allergic contact dermatitis. The standard panel consists of two tape strips, panel 1, with 11 allergen patches and a negative control and panel 2, with 12 allergen patches. T.R.U.E. TestTM panels 1 and 2 contain 23 of the most frequent contact allergens. With the 23 allergens the test currently consists of, it is possible to detect about 60-70% of contact allergic reactions. Thus, there is a need for expanding the number of allergens included in T.R.U.E.Test in order to detect more contact allergic reactions. Bacitracin is one of these allergens, and the purpose of this study is to determine a concentration for the patch by using a bacitracin dilution series.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Contact Dermatitis
Keywords
Allergic contact dermatitis, Patch testing, bacitracin

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
Double
Allocation
Non-Randomized
Enrollment
20 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
bacitracin (allergen)
Primary Outcome Measure Information:
Title
Skin reaction to the patch test after 72-96 hours and after 7 days
Secondary Outcome Measure Information:
Title
Evaluation of safety including late and persistent responses
Title
Evaluation day 3/4, day 7 and day 21

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Positive bacitracin patch test within the latest 5 years. Age greater than or equal to 18 years. Signed informed consent. Exclusion Criteria: Topical treatment with corticosteroids or immunosuppressives during the latest 7 days on the test area or near the test area. Systemic treatment with corticosteroids or immunosuppressives during the latest 7 days. Treatment with ultraviolet (UV)-light during the latest 3 weeks. Widespread active dermatitis or dermatitis on test area. Breast-feeding or pregnancy. Females of childbearing potential must demonstrate a negative pregnancy test before inclusion in the study. Subjects not able to cooperate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joseph Fowler, Prof.
Organizational Affiliation
Mekos Laboratories AS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dermatological Clinic (Joseph Fowler MD)
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States

12. IPD Sharing Statement

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Clinical Evaluation of Bacitracin

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