- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01494948
Innate Immunity and the Allergic Response
January 7, 2014 updated by: Medical College of Wisconsin
The purpose of this study is to determine if a certain cell type (the CD49d+ neutrophil) is associated with the presence or development of allergic disease.
Study Overview
Detailed Description
A specific subset of neutrophils (CD49d+) will be recruited to the nasal tissue of individuals with allergic disease, and that these cells will also be found in the peripheral blood of allergic subjects.
Normal subjects (those without atopy) and those treated for atopic disease will lack the presence of these cells.
Study Type
Interventional
Enrollment (Actual)
36
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Must give written informed consent before any study related activity is performed
- Male and female adult and adolescent patients aged ≥18 years and ≤ 65 years.
- Allergic or non-allergic subjects as proven by allergy skin tests in the past 2 years.
Exclusion Criteria:
- The presence of any of these diseases: Atopic dermatitis, persistent controlled asthma, any level of severity of uncontrolled asthma, immunodeficiency or suspected immunodeficiency, any co-morbid disease (cardiac, congenital, diabetes, renal, gastrointestinal, hematologic, and oncologic).
- Any prior history of immunodeficiency, cardiac, congenital, diabetes, renal, gastrointestinal, hematologic, or oncologic disease.
- The use of any intranasal and inhaled corticosteroids within the last month.
- Current therapy with any medication other than as needed over-the-counter medications or as-needed (not scheduled) antihistamine use.
- Current pregnancy.
- Women of childbearing potential not using an acceptable birth control method, as well as women who are breastfeeding
- Patients with severe medical condition(s) that in the view of the investigator prohibits participation in the study (specify as required)
- Use of any other investigational agent in the last 30 days
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: placebo
skin test negative
|
nasal challenges with antigen to which they are sensitive to
|
|
Active Comparator: allergic
Skin test positive
|
nasal challenges with antigen to which they are sensitive to
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Increase in percentage of CD49d expressing neutrophils in nasal lavage post allergen challenge.
Time Frame: 1month
|
Nasal lavage on atopic and non-atopic adult subjects will be performed at baseline and following an allergen challenge.
The frequency of CD49d expressing neutrophils in the lavage fluid will be determined by flow cytometry analysis, and the change in this frequency will be correlated with atopic status and allergen challenge.
This is an observational study, procedures performed are not intended to impact the outcome of the individual participants.
|
1month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in immune cell numbers in the nasal lavage following allergen challenge
Time Frame: 1 month
|
The numbers of neutrophils, CD49d+ neutrophils, lymphocytes, dendritic cells, and macrophages in the nasal lavage will be determined before and after allergen challenge.
The outcome will be correlation of these changes with allergy status and any clinical symptoms of the allergen challenge (i.e., sneezing).
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mitchell Grayson, MD, Medical College of Wisconsin
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2012
Primary Completion (Actual)
March 1, 2013
Study Completion (Actual)
March 1, 2013
Study Registration Dates
First Submitted
November 7, 2011
First Submitted That Met QC Criteria
December 15, 2011
First Posted (Estimate)
December 19, 2011
Study Record Updates
Last Update Posted (Estimate)
January 8, 2014
Last Update Submitted That Met QC Criteria
January 7, 2014
Last Verified
January 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- 221035-2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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