Clinical Trials Directory

Trials / Completed

CompletedNCT06137495

Immunoblot, Chemiluminescence and ImmunoCap Allergen Specific IgE Evaluation of in Allergic Rhinitis Patients

Immunoblot and Chemiluminescence Assays Versus ImmunoCap: Evaluation of Allergen Specific IgE in Egyptian House Dust Mites Allergic Rhinitis Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
84 (actual)
Sponsor
Zagazig University · Other Government
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

In the present study the investigators assay house dust mites (HDMs) IgE in sera of allergic rhinitis patients (AR) using immunoblotting, chemiluminescence, and ImmunoCAP assays to compare between the accuracy of both immunoblotting and chemiluminescence assays, and ImmunoCAP as gold standard.

Detailed description

All allergic rhinitits patients who were monosensitized to mixed HDMs, identified by SPT, will be subjected to complete history taking and assessment of the inclusion and exclusion criteria, performance of skin prick test and measurement of total serum IgE, measurement of specific IgE by Chemiluminescence Immunoassa, immunoblot assay and ImmunoCAP™ Phadiatop™. The patients will be followed-up for 6 months.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTSensitization to House dust mitesThe SPT is performed at the time of diagnosis and after six-months follow-up period. Serum specific IgE is measured by immunoblotting, chemiluminescence, and ImmunoCAP assays

Timeline

Start date
2020-12-01
Primary completion
2023-06-30
Completion
2023-06-30
First posted
2023-11-18
Last updated
2023-11-22

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06137495. Inclusion in this directory is not an endorsement.