Overview

The Diurnal and Nocturnal Effect of Pilocarpine on Intraocular Pressure and Ocular Perfusion Pressure

Status:
Completed
Trial end date:
2018-02-21
Target enrollment:
0
Participant gender:
All
Summary
The aim of this study will be to determine the effects of pilocarpine as an adjunct medication to latanoprost monotherapy at multiple intervals throughout a 24-hour period and compare these effects to latanoprost alone.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Colorado, Denver
Treatments:
Latanoprost
Pilocarpine
Criteria
Inclusion Criteria:

- Current confirmed diagnosis of:

- open angle glaucoma, or

- ocular hypertension including pigment dispersion glaucoma, and

- pseudoexfoliation glaucoma.

- Current use of topical latanoprost once a day in both eyes for at least 6 weeks

- any race/ethnicity

Exclusion Criteria:

- Females who are currently pregnant or planning to become pregnant during the study
period

- Diagnosis of any other form of glaucoma other than open-angle

- Intraocular pressure readings of <14mmHg in either eye when measured during routine
office visit in the past 12 months.

- Schaffer angle grade < 2 in either eye by gonioscopy

- Intraocular surgery within 6 months or laser within 3 months

- History of retinal tear or detachment in either eye

- Active iritis in either eye as determined by most recent eye examination

- Patients who smoke or have irregular daily sleep patterns

- Patients who have started or changed glucocorticoids therapy in the last 3 months

- Patients who are currently using medical or recreational marijuana

- Any use of a non-FDA approved medication for glaucoma in the last 3 months