Study Results
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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COMPLETED
NA
2000 participants
INTERVENTIONAL
2013-02-28
2016-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Prick to prick
Prick to prick test
Interventions
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Prick to prick test
Eligibility Criteria
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Inclusion Criteria
* consent obtained from patients or their parents/legal representative
Exclusion Criteria
* antihistamine drugs taken before testing
* pregnant women
* vulnerable patients according to French regulation
2 Years
ALL
Yes
Sponsors
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University Hospital, Montpellier
OTHER
Responsible Party
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Locations
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University Hospital of Montpellier
Montpellier, , France
Countries
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Other Identifiers
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UF 9045
Identifier Type: -
Identifier Source: org_study_id
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