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

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

34 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-08-31

Study Completion Date

2009-09-30

Brief Summary

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The study was designed to evaluate the pattern of seasonal allergic signs and symptoms consistent with ongoing ocular allergic inflammation during ragweed season. It was hypothesized that a pattern of ongoing ocular allergic inflammation existed in certain subjects.

Detailed Description

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Subjects who had a positive skin test to ragweed within 24 months of Visit 1 were instructed to complete a diary, which assessed their allergic signs and symptoms 3 times a day for 4 weeks. During the in-office visits, subjects were asked to completed a quality of life questionnaire, as well as a retrospective and/or prospective eye allergy questionnaire.

Conditions

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Allergic Conjunctivitis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Subjects must:

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

* Subjects may not:

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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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ORA, Inc.

INDUSTRY

Sponsor Role lead

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

Site Status

Countries

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United States

Other Identifiers

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08-003-26

Identifier Type: -

Identifier Source: org_study_id

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