Status:

UNKNOWN

e-ITAG Allergen Immunotherapy in the Management of Allergic Asthma

Lead Sponsor:

General Administration of Military Health, Tunisia

Conditions:

Study the Efficacy of ITA in Patients With Allergic Asthma or Allergic Rhinitis or Allergic Rhinitis Compared With Conventional Treatment

Eligibility:

All Genders

5-65 years

Brief Summary

Allergy is defined as a specific abnormal and excessive reaction of the immune system to exposed allergen . This reaction is reproducible with each new exposure allergen . A recent study by The Europ...

Detailed Description

This is a prospective, observationel study conducted in Pneumology Department at the Military Hospital in collaboration with the Immunology Laboratory We followed patients in 2 groups: Group 1: pati...

Eligibility Criteria

Inclusion

  • Inclusion Criteria Patients with symptoms of Asthma or moderate or severe persistent allergic rhinitis allergic rhinitis, with a positive prick test or specific IgE assay demonstrating the presence of allergens (1 or 2 allergens). A significant impact on the patient's quality of life Rhinitis associated with tracheitis or mild-to-moderate asthma. Patients with poorly controlled asthma despite optimal treatment Ineffective drug treatment Patients willing to adhere to our research protocol
  • Exclusion Criteria:
  • Patients with multi-allergenic asthma (more than 2 allergens) Pregnancy (at the time of ITA initiation). Autoimmune disease Immunosuppressive treatment Poorly controlled asthma HIV infection Cancer Severe psychiatric disorders. Cardiovascular diseases with a risk of complications during administration of adrenaline. Use of beta-blockers. Treatment with ACE inhibitors. Persistent lesions of the oral mucosa (chronic oral aphthosis periodontitis, etc.). Worsening of rhinitis. Acute febrile state. Recent administration of another vaccine (in this case, the ITA should not be administered on the same day).
  • ITA should not be administered on the same day).

Exclusion

    Key Trial Info

    Start Date :

    March 1 2023

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    March 30 2024

    Estimated Enrollment :

    300 Patients enrolled

    Trial Details

    Trial ID

    NCT06021912

    Start Date

    March 1 2023

    End Date

    March 30 2024

    Last Update

    September 1 2023

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Military Hospital of Tunis

    Tunis, Montfleury, Tunisia, 1008