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Criteria Used by Health Professionals on the Selection of Allergen Immunotherapy in Real Clinical Practice (CHOICE)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Completed

Conditions

Allergen Immunotherapy

Study type

Observational

Funder types

Other

Identifiers

NCT04038268
RECHMPL19_0361

Details and patient eligibility

About

Background : Allergen Immunotherapy (AIT) is the only etiological treatment for allergic respiratory diseases. In order to improve the competence on the use of AIT, it is important to extend the investigator's knowledge on its use in routine clinical practice, outside the experimental setting of clinical trials, in real life population of patients receiving AIT.

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).

Enrollment

400 patients

Sex

All

Ages

5+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with IgE mediated respiratory allergy
  • 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

  • Patients who refuse to give their informed consent
  • Food immunotherapy
  • Venom Immunotherapy

Trial design

400 participants in 2 patient groups

Patients
Description:
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
Prescribers
Description:
Doctors who are currently prescribing AIT as part of their regular clinical practice

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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