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Clinical Trials/NCT01937494
NCT01937494
Completed
Not Applicable

Are Technicians Showing Bronchial Hyperreactivity Able to Safely Perform Bronchial Provocation Tests?

Centre Hospitalier Universitaire Saint Pierre1 site in 1 country13 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
histamine-benzylic alcohol (magistral preparation)
Conditions
Asthma
Sponsor
Centre Hospitalier Universitaire Saint Pierre
Enrollment
13
Locations
1
Primary Endpoint
spirometric values in patients exposed passively to histamine during BHR challenge
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Bronchial hyperresponsiveness consists in excessive response to bronchial stimuli.Bronchial challenge test is used to confirm/exclude asthma (metacholine or histamine).Protection are used to avoid passive exposure of the technicians performing the test, despite the absence of evidence that they could develop a bronchoconstriction even if they suffer from BHR.The purpose of the study is to determine if patients with a high level of bronchial hyperreactivity and exposed passively to histamine during a bronchial challenge, are developing a bronchoconstriction, when placed in the same conditions that the technicians performing these tests.

Detailed Description

Bronchial hyperresponsiveness (BHR) consists in excessive response to bronchial stimuli.Bronchial challenge test is used to confirm/exclude asthma.BHR is also present in other diseases such as allergic rhinitis, Chronic Obstructive pulmonary disease,heart failure.. Thes test is performed with metacholine or histamine with spirometric documented response to incremental doses.Protection are used to avoid passive exposure of the technicians performing the test, despite the absence of evidence that they could develop a bronchoconstriction if they suffer from BHR. The purpose of the study is to determine if patients, newly diagnosed with a high level of bronchial hyperreactivity and exposed passively to histamine during a bronchial challenge, are reacting to histamine when placed in the same conditions that the technicians performing these tests.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
May 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Centre Hospitalier Universitaire Saint Pierre
Responsible Party
Principal Investigator
Principal Investigator

Marie Bruyneel

CCA, pneumologie

Centre Hospitalier Universitaire Saint Pierre

Eligibility Criteria

Inclusion Criteria

  • adult patients with positive histamine challenge test (first dose)

Exclusion Criteria

  • other active respiratory disease

Arms & Interventions

asthma patients

patients who show a positive response at the first dos of histamine challenge test will be enrolled

Intervention: histamine-benzylic alcohol (magistral preparation)

Outcomes

Primary Outcomes

spirometric values in patients exposed passively to histamine during BHR challenge

Time Frame: 1 hour

Study Sites (1)

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