Trials / Completed
CompletedNCT02754570
The Diurnal and Nocturnal Effect of Pilocarpine on Intraocular Pressure and Ocular Perfusion Pressure
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- University of Colorado, Denver · Academic / Other
- Sex
- All
- Age
- 18 Years – 89 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
This study plans to learn more about the effect of pilocarpine on intraocular pressure and ocular perfusion pressure for a full twenty-four hour period. In this study, the investigators seek to better characterize the knowledge base of the intraocular pressure (IOP) lowering effects of pilocarpine in patients with open angle glaucoma or ocular hypertension who are currently taking latanoprost. The goal is to define the potential additive effect of pilocarpine throughout a 24-hour period, not only for IOP, but for ocular perfusion pressure (defined as 2/3\[diastolicBP + 1/3(systolicBP - diastolicBP)\] - IOP). These data will allow to expand current knowledge of the effects of pilocarpine and help determine if this medication has a useful role as an adjunctive treatment in glaucoma.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Pilocarpine | Pilocarpine will be administered 4 times in addition to latanoprost. |
Timeline
- Start date
- 2016-07-01
- Primary completion
- 2017-12-01
- Completion
- 2018-02-21
- First posted
- 2016-04-28
- Last updated
- 2019-11-07
- Results posted
- 2019-11-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02754570. Inclusion in this directory is not an endorsement.