Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Alcon Research
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Clinical diagnosis of ocular hypertension, primary open-angle glaucoma or pigmentary glaucoma;
Intraocular pressure (IOP) of between 19 to 35 mmHg at any time of the day in at least one eye (designated as the study eye);
On a stable medication regimen for IOP reduction one week prior to the screening visit;
Best corrected visual acuity better than 20/200 (Snellen) or 1.0 (logMAR) in each eye;
Sign informed consent;
You may not be if
Known medical history of allergy, hypersensitivity or low tolerance to any of the components of DuoTrav®;
Any abnormality that would preclude the reliable performance of applanation tonometry in either eye;
Infection in either eye;
Conventional or laser intraocular surgery in either eye 3 months prior to screening visit;
Risk for visual field or visual acuity worsening, in the opinion of the investigator;
Women of childbearing potential;
Pregnant or lactating women;
Any condition that, in the opinion of the principal investigator, could interfere with participation in the study, or that could present a risk to the participant.
Participation in another clinical study within 30 days before the screening visit;
