Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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16 December 2017 |
Main ID: |
NCT03019237 |
Date of registration:
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10/01/2017 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Effect of Intranasal Anti-IgE Antibodies on IgE Production
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Scientific title:
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The Effect of Intranasal Application of Anti-IgE Antibodies on IgE Production in Patients Suffering From Seasonal Allergic Rhinitis - a Pilot Study |
Date of first enrolment:
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November 2012 |
Target sample size:
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15 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT03019237 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Basic Science. Masking: Triple (Participant, Investigator, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Austria
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Contacts
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Name:
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Verena Niederberger, MD |
Address:
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Telephone:
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Email:
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Affiliation:
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Medical University of Vienna |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
birch pollen allergy
Exclusion Criteria:
history of anaphylaxis autoimmune diseases treatment with corticosteroids, antihistamines,
immunosuppressant drugs, beta-blockers significant medical conditions pregnancy or
lactation
Age minimum:
18 Years
Age maximum:
60 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Allergy
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Intervention(s)
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Other: intranasal saline
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Drug: anti-IgE
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Other: intranasal allergen
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Primary Outcome(s)
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change of allergen-specific IgE
[Time Frame: 8 weeks]
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Secondary Outcome(s)
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changes in total IgE
[Time Frame: 8 weeks]
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Secondary ID(s)
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2012-004193-25
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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