Assessment of Alcon's Ocular Image Quantification System
Completed · Phase 4
Conditions studied: Allergic Conjunctivitis
In brief
The purpose of this study was to evaluate ocular responses with different allergen provocation methods.
Key facts
- Study ID
- NCT01282138
- Run by
- Alcon Research
- People needed
- 13
- Starts
- 2010-12-01
- Expected to finish
- 2011-03-01
- Last updated by the study team
- 2012-12-18
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- History of allergic conjunctivitis;
- Active signs and symptoms of ocular allergies;
- Other protocol-defined inclusion criteria may apply.
You may not qualify if…
- History of dry eye;
- Presence of ocular infection;
- Presence of severe or serious ocular conditions;
- Symptoms of allergic conjunctivitis;
- Use of topical or systemic ocular medications as specified in protocol;
- Ocular surgery or laser surgery within 6 months of study start;
- Unwilling to discontinue contact lens wear 72 hours prior to Visit 1 and during study period;
- Other protocol-defined exclusion criteria may apply.
Where it is running
- Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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