A Single-Center Evaluation of the Pattern of Allergic Signs and Symptoms During 4 Weeks in Ragweed Season
NCT ID: NCT00982163
Last Updated: 2009-09-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
34 participants
OBSERVATIONAL
2008-08-31
2009-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
1. be willing and able to read, sign, and date the informed consent and HIPAA documents prior to initiation of Visit 1 procedures or exams;
2. be at least 18 years of age;
3. be willing to avoid disallowed medication, such as anti-allergy therapies
4. have a positive history of ocular allergies and a positive skin test reaction to ragweed within the past 24 months;
5. have a calculated logMAR visual acuity score using the ETDRS Chart of 0.60 or better in each eye at Visit 1;
Exclusion Criteria
1. have preauricular lymphadenopathy or any ocular condition that could affect study parameters (particularly, clinically significant blepharitis, follicular conjunctivitis and iritis);
2. have had any ocular infection within the last 30 days;
3. have a positive diagnosis of moderate to severe dry eye syndrome (i.e., requiring daily use of artificial tears);
4. wear contact lenses to each office visit; Note: Subjects will be allowed to use cold compresses.
18 Years
ALL
No
Sponsors
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ORA, Inc.
INDUSTRY
Responsible Party
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Ophthalmic Research Associates
Principal Investigators
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H. Jerome Crampton, M.D.
Role: PRINCIPAL_INVESTIGATOR
ORA, Inc.
Locations
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ORA, Inc.
North Andover, Massachusetts, United States
Countries
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Other Identifiers
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08-003-26
Identifier Type: -
Identifier Source: org_study_id
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