Status:

TERMINATED

Interest of Nasal Provocation Tests for Diagnosis of House Mites Allergic Rhinitis

Lead Sponsor:

Centre Hospitalier Régional Metz-Thionville

Collaborating Sponsors:

University Hospital, Strasbourg, France

Centre Hospitalier de Verdun

Conditions:

Mite Allergy

Respiratory Disease

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

The aim of this clinical trial is to compare the positive predictive value of the combination rapid nasal provocation test (RNTP) + skin tests (TC) + specific immunoglobulins E (IgEs) to the combinati...

Detailed Description

Allergic rhinitis due to house dust mites (AAR) is a common condition which impairs the quality of life of patients and which can be responsible for complications such as the development of asthma. Th...

Eligibility Criteria

Inclusion

  • Patient over 18 years old,
  • Patient with persistent mild to severe or moderate to severe intermittent rhinitis according to ARIA criteria, suspicion of allergic rhinitis to dust mites, and a positive skin test for mites and / or a positive mite specific IgE assay
  • Patient having signed a free and informed consent

Exclusion

  • Pregnant or breastfeeding women
  • Patients under guardianship or curatorship
  • Patients under legal protection
  • Patients not affiliated to a social security scheme
  • Contraindications to performing a RNPT
  • Active ENT or respiratory infections.
  • Allergy in acute phase
  • History of anaphylaxis due to the allergen involved.
  • Unstabilized asthma and other obstructive pathologies.
  • Severe general illnesses in evolution.
  • Hypersensitivity to one of the components of the product
  • Simultaneous treatment with beta-blockers or angiotensin-converting enzyme (ACE) inhibitors,
  • Presence of an excessive degree of sensitization (e.g. history, excessive skin reactions),
  • Contraindications to immunotherapy:
  • Asthma (uncontrolled) or severe \[FEV \< 70% of the theorical value (after appropriate drug treatment) at the beginning of the treatment\].
  • Severe asthma exacerbation in the last 3 months
  • Active autoimmune diseases
  • Malignant tumors
  • Pregnancy (initiation of venereal disease)
  • AIDS
  • Treatment with beta-blockers, including eye drops

Key Trial Info

Start Date :

March 7 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 5 2024

Estimated Enrollment :

8 Patients enrolled

Trial Details

Trial ID

NCT04915352

Start Date

March 7 2022

End Date

July 5 2024

Last Update

August 9 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

1

CHR Metz Thionville/Hopital de Mercy

Metz, Grand Est, France, 57085