- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00985296
Conjunctival Allergen Challenge (CAC) Following Allergen Exposure in the Allergen BioCube (ABC) (ABC CAC)
September 20, 2010 updated by: ORA, Inc.
A Pilot Study Evaluating the Effect of Conjunctival Allergen Challenge (CAC) on Nasal and Ocular Allergic Symptoms Following Allergen Exposure in the Allergen BioCube (ABC) in Subjects With Seasonal Allergic Rhinoconjunctivitis
To evaluate the effect of Conjunctival Allergen Challenge (CAC) with Dust Mites on nasal and ocular allergic symptoms following allergen exposure in the Allergen BioCube (ABC).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Anticipated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Massachusetts
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Andover, Massachusetts, United States, 01810
- ORA, Inc.
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-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Subjects will be 18 years of age or older with a positive history of ocular and nasal allergy and a positive skin test reaction to ragweed within the past 24 months.
Description
Inclusion Criteria:
- be at least 18 years of age;
- if female, cannot be pregnant or nursing;
- have a history of ocular and nasal allergy;
- have a positive skin test reaction to ragweed within the past 24 months;
- may/may not have a positive skin test reaction to dust mites within the past 24 months
Exclusion Criteria:
- have a history of mild persistent, moderate or severe asthma within the preceding 5 years according to the National Heart, Blood and Lung Institute classification;
- have a compromised lung function;
- have any ocular condition that could affect the subject's health or the study parameters;
- have any presence of active ocular or sinus infection;
- have significant nasal conditions;
- have any significant illness that could be expected to interfere with the subject's health or with the study parameters;
- use specified disallowed medications (topical, topical ophthalmic, systemic and/or injectable treatments and all anti-allergy therapies) during the study or appropriate pre-study washout period;
- have used an investigational drug or device within 30 days of starting the study or be concurrently enrolled in another investigational drug or device study within 30 days of the study;
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
Cohorts and Interventions
Group / Cohort |
|---|
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Ragweed+ Dust Mite+ CAC w/ DM
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Ragweed + Dust Mite + CAC w/Saline
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Ragweed + Dust Mite - CAC
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Ocular Itching
Time Frame: At specified timepoints for up to 2 hours
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At specified timepoints for up to 2 hours
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Conjunctival Redness
Time Frame: At specified timepoints for up to 2 hours
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At specified timepoints for up to 2 hours
|
|
Total Ocular Symptom Score (TOSS) of ocular itching and redness
Time Frame: At specified timepoints for up to 2 hours
|
At specified timepoints for up to 2 hours
|
|
Total Nasal Symptom Score (TNSS) of nasal symptoms
Time Frame: At specified timepoints for up to 2 hours
|
At specified timepoints for up to 2 hours
|
|
Nasal itching, Sneezing, Rhinorrhea, and Nasal Congestion
Time Frame: At specified timepoints for up to 2 hours
|
At specified timepoints for up to 2 hours
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Ciliary and episcleral redness
Time Frame: At specified timepoints for up to 2 hours
|
At specified timepoints for up to 2 hours
|
|
Chemosis
Time Frame: At specified timepoints for up to 2 hours
|
At specified timepoints for up to 2 hours
|
|
Lid Swelling
Time Frame: At specified timepoints for up to 2 hours
|
At specified timepoints for up to 2 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Paul Gomes, MS, ORA, Inc.
- Principal Investigator: Henry J. Crampton, MD, ORA, Inc.
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
September 1, 2009
Primary Completion (Actual)
August 1, 2010
Study Completion (Actual)
August 1, 2010
Study Registration Dates
First Submitted
September 25, 2009
First Submitted That Met QC Criteria
September 25, 2009
First Posted (Estimate)
September 28, 2009
Study Record Updates
Last Update Posted (Estimate)
September 21, 2010
Last Update Submitted That Met QC Criteria
September 20, 2010
Last Verified
September 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09-003-24
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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