Criteria Used by Health Professionals on the Selection of Allergen Immunotherapy in Real Clinical Practice
NCT ID: NCT04038268
Last Updated: 2020-12-29
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
400 participants
OBSERVATIONAL
2019-09-01
2020-09-30
Brief Summary
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Objective: To evaluate the clinical criteria used by treating clinicians and by the patients themselves, when establishing AIT as treatment in a patient with respiratory disease caused by an IgE-dependent-hypersensitivity to aeroallergens Methods: In 6 country (Denmark, France, Germany, Norway, Spain \& Sweden), the national coordinator will be directly responsible for selection of Survey Doctor's participants (Investigators).
During 12 months:
* Firstly, each investigator will complete the Survey Doctor, online, on SurveyMonkey platform to explain what are the key drivers in Allergen Immunotherapy (AIT) selection (Doctors' Questionnaire, DQ).
* On the other hand, at each AIT prescription to a patient, doctors will complete the Survey Patient, on the same platform, to explain how and why they have chosen this type of AIT (Patients' Questionnaire, PQ).
Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Patients
Adults and children, males and females, with IgE mediated pollen, house dust mites, animal dander and moulds respiratory allergy who will initiate aeroallergen AIT, either SCIT, SLIT-drops or SLIT-tablets according to real life clinical standards of practice
No interventions assigned to this group
Prescribers
Doctors who are currently prescribing AIT as part of their regular clinical practice
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients who will initiate any type of aeroallergen AIT according to real life clinical standards of practice
* Any type of aeroallergen for AIT will be included : pollen, house dust mite, animal, dander, moulds
* Patient who is under the care of the Doctor participating in the survey
Exclusion Criteria
* Food immunotherapy
* Venom Immunotherapy
5 Years
ALL
No
Sponsors
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University Hospital, Montpellier
OTHER
Responsible Party
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Principal Investigators
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Pascal Demoly
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Montpellier
Locations
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Uhmontpellier
Montpellier, , France
Countries
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Other Identifiers
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RECHMPL19_0361
Identifier Type: -
Identifier Source: org_study_id