- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01156038
Atopy Patch Test in Normal Population : Pilot Study
July 1, 2010 updated by: Mahidol University
Atopy patch test in normal population
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The initial diagnostic work up of suspected food allergy includes patient's history, skin prick test (SPT), measurement of food specific immunoglobulin E (IgE) with serological assays, and more recently the atopy patch test.
A positive SPT seems to reflect early reactions to food challenges, whereas the atopy patch test has a high diagnostic efficacy for late phase clinical reactions.
The purpose of this study was to evaluate atopy patch test reaction in non-atopic population.
Study Type
Interventional
Enrollment (Actual)
15
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bangkok, Thailand, 10700
- Department of Pediatrics, Siriraj hospital, Mahidol University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy volunteer
- Age 18-40 yrs
- Volunteer sign for informed consent
Exclusion Criteria:
- who have dermographism
- who have chronic disease eg.autoimmune disease, immune deficiency, cancer or allergic disease
- pregnant women
- who have severe eczema
- who receive antihistamine, topical steroid and systemic steroid > 20 mg/day within 7 days prior study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Atopy patch test
Atopy patches were applied on healthy volunteer's back for 48 hrs then the patches were removed.
Reaction was evaluated 48 and 72 hrs after applying atopy patch test
|
Atopy patches used with food lyophilized allergen and commercial allergen were placed on back of subjects for 48 hrs then atopy patches were taken off.
Subjects should return to evaluate reaction one day later(72 hrs after applying atopy patch test)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reaction of atopy patch test
Time Frame: 3 days
|
To evaluate outcome of atopy patch test reaction in non-atopic subject
|
3 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparisons atopy patch test reaction between lyophilized allergen and commercial allergen
Time Frame: 3 days
|
To compare outcome of atopy patch test reaction using lyophilized allergen and commercial allergen
|
3 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Nualanong Visitsunthorn, Professor, Mahidol University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2010
Primary Completion (Actual)
May 1, 2010
Study Completion (Actual)
May 1, 2010
Study Registration Dates
First Submitted
May 16, 2010
First Submitted That Met QC Criteria
July 1, 2010
First Posted (Estimate)
July 2, 2010
Study Record Updates
Last Update Posted (Estimate)
July 2, 2010
Last Update Submitted That Met QC Criteria
July 1, 2010
Last Verified
July 1, 2010
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 599/2552(EC4)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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