Overview

Pilocarpine and Brimonidine in Patients With Monofocal Lenses

Status:
Unknown status
Trial end date:
2019-12-31
Target enrollment:
0
Participant gender:
All
Summary
The current study aims to assess the use of pilocarpine and brimonidine to improve near visual acuity in patietns with monofocal intraocular lenses. Thirty-three subjects with be enrolled and baseline visual acuity with be measured at near and distance. This will be compared to visual acuity after drop administration over 6 hours. A quality of life questionnaire will also be evaluated.
Phase:
Early Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Massachusetts Eye and Ear Infirmary
Treatments:
Brimonidine Tartrate
Pilocarpine
Criteria
Inclusion Criteria:

- Individuals must meet all of the inclusion criteria in order to be eligible to
participate in the study. Men and women between ages 60 years and above with monofocal
intraocular lenses bilaterally corrected for distance and +/- 0.5D sphere vision who
need only +/- 2.5 D correction for reading. Given the age group selected only post
menopausal women will be evaluated.

Exclusion Criteria:

- Individuals meeting any of the exclusion criteria at baseline will be excluded from
study participation including: allergies to proparacaine, pilocarpine or brimonidine,
eye infection or inflammation, glaucoma, retinal tear or retinal disease, eye surgery
within the past 30 days, use of eye drops within the last seven days, participated in
any other research study within the past 30 days. Patients using contact lenses.