Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Alcon Research
Age
21–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Sign Informed Consent.
21 years of age or older.
Able to follow instructions and willing to attend required study visits.
Clinical diagnosis of ocular hypertension, primary open-angle, or pigment dispersion glaucoma in at least one eye (qualifying eye).
Intra-ocular pressure (IOP) considered to be safe in both eyes in such a way that should assure clinical stability of vision and the optic nerve throughout the trial.
Must have best corrected visual acuity of 6/60 (6/60 Snellen, 1.0 LogMAR) or better in each eye.
You may not be if
Presence of other primary or secondary glaucomas not listed in inclusion criterion.
Presence of corneal dystrophies.
Concurrent infectious/noninfectious conjunctivitis, keratitis or uveitis in either eye.
Intraocular conventional surgery or laser surgery in qualifying eye(s) less than three months prior to Visit 1.
Risk of visual field or visual acuity worsening as a consequence of participation in the trial, in the investigator's best judgment.
Women of childbearing potential not using reliable means of birth control.
Women who are pregnant or lactating.
Participation in any other investigational study within 30 days prior to Visit 1.
Current or anticipated use of systemic corticosteroids, by any route except inhaled, for greater than two weeks during the trial.
Severe allergic rhinitis
History of ocular herpes simplex.
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