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
Diagnosis of open-angle glaucoma or ocular hypertension;
Inadequate control with beta-blocker or prostaglandin monotherapy and starting therapy with travoprost 0.004% and timolol 0.05%;
Intraocular pressure (IOP) at the screening visit in at least one eye ≥ 19 mmHg but not exceeding 36 mmHg in either eye;
You may not be if
Females of childbearing potential currently pregnant, breastfeeding, or not taking control measures to prevent pregnancy;
Not currently receiving treatment for lowering IOP with beta-blockers or prostaglandin analogs;
Currently on therapy or was in therapy with another investigational agent within 30 days prior to the baseline visit;
History of chronic or recurrent severe inflammatory eye disease, or history of ocular trauma within the past six (6) months, or history of ocular infection or ocular inflammation within the past three (3) months in either eye;
History of clinically significant or progressive retinal disease or history of any other severe ocular pathology in either eye that would preclude the administration of a topical prostaglandin analogue;
History of severe or serious hypersensitivity to prostaglandin drugs or their analogues, to topical or systemic beta-blockers, or to any components of the study medication;
Intraocular surgery within the past six (6) months or ocular laser surgery within the past three (3) months as determined by patient history and/or examination in either eye;
Any abnormality preventing reliable applanation tonometry of either eye;
Best-corrected visual acuity worse than 20/30 Snellen in either eye;
Use of any additional topical or systemic ocular hyposensitive medication during the study;
Clareo Health | Adherence Assessment With Travalert Dosing Aid
