The Diurnal and Nocturnal Effect of Simbrinza and Timolol on Intraocular Pressure and Ocular Perfusion Pressure
Last updated on April 2022Recruitment
- Recruitment Status
- Completed
Inclusion Criteria
- Diagnosis of open angle glaucoma or ocular hypertension including pigment dispersion glaucoma and pseudoexfoliation glaucoma.
- Age ≥ 18 years, of either gender, or any race/ethnicity
- Diagnosis of open angle glaucoma or ocular hypertension including pigment dispersion glaucoma and pseudoexfoliation glaucoma.
- Age ≥ 18 years, of either gender, or any race/ethnicity
Exclusion Criteria
- Schaffer angle grade < 2 in either eye by gonioscopy
- Patients currently taking oral beta blocker therapy
- Females who are currently pregnant or planning to become pregnant during the study period
- ...
- Schaffer angle grade < 2 in either eye by gonioscopy
- Patients currently taking oral beta blocker therapy
- Females who are currently pregnant or planning to become pregnant during the study period
- Patients who are currently using medical or recreational marijuana
- Intraocular surgery within 6 months or laser within 3 months
- Diagnosis of any other form of glaucoma other than open-angle
- Inability to safely discontinue all ocular medications for 6 weeks
- History of allergy or intolerance to topical carbonic anhydrase inhibitors, or alpha-agonists
- Patients who have started or changed glucocorticoids therapy in the last 3 months
- Contraindications to beta blockers (see below)
- Any use of a non-FDA approved medication for glaucoma in the last 3 months
- Patients who smoke or have irregular daily sleep patterns
Summary
- Conditions
- Ocular Hypertension
- Open Angle Glaucoma
- Pigment Dispersion Syndrome
- Pseudoexfoliation Glaucoma
- Type
- Observational
- Design
- Observational Model: Cohort
- Time Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
Intraocular pressure (IOP) is a major risk factor for the development of glaucoma. In addition, it is the only modifiable factor in the prevention and subsequent treatment of glaucomatous optic neuropathy. Most clinicians only have access to a single IOP measurement during a patient visit that may o...
Intraocular pressure (IOP) is a major risk factor for the development of glaucoma. In addition, it is the only modifiable factor in the prevention and subsequent treatment of glaucomatous optic neuropathy. Most clinicians only have access to a single IOP measurement during a patient visit that may only occur once every four months. These snapshots in time are probably not adequate for the optimal management of glaucoma. Diurnal IOP curves can provide a better estimate of each patient's individual IOP variation throughout the day. However diurnal curves do not typically cover another crucial time, the nocturnal period. Glaucomatous eyes have been shown to have different IOP curves during the nocturnal period compared to healthy controls. In addition, different classes of glaucoma drugs have variable IOP lowering effects during the nocturnal hours compared to the diurnal/wake period. For example, the betablocker timolol was shown to lower IOP during daytime hours but failed to lower IOP during the nocturnal period in the habitual position. Similarly, the alpha-agonist brimonidine failed to lower IOP overnight after significantly lowering IOP during the diurnal period. On the other hand, the prostaglandin analogues, including latanoprost and travoprost, lowered IOP throughout the diurnal and nocturnal periods although nocturnal lowering appears less than the daytime hours. Therefore it is crucial to determine an accurate IOP curve for each form of medication during both wake and sleep hours.
Inclusion Criteria
- Diagnosis of open angle glaucoma or ocular hypertension including pigment dispersion glaucoma and pseudoexfoliation glaucoma.
- Age ≥ 18 years, of either gender, or any race/ethnicity
- Diagnosis of open angle glaucoma or ocular hypertension including pigment dispersion glaucoma and pseudoexfoliation glaucoma.
- Age ≥ 18 years, of either gender, or any race/ethnicity
Exclusion Criteria
- Schaffer angle grade < 2 in either eye by gonioscopy
- Patients currently taking oral beta blocker therapy
- Females who are currently pregnant or planning to become pregnant during the study period
- ...
- Schaffer angle grade < 2 in either eye by gonioscopy
- Patients currently taking oral beta blocker therapy
- Females who are currently pregnant or planning to become pregnant during the study period
- Patients who are currently using medical or recreational marijuana
- Intraocular surgery within 6 months or laser within 3 months
- Diagnosis of any other form of glaucoma other than open-angle
- Inability to safely discontinue all ocular medications for 6 weeks
- History of allergy or intolerance to topical carbonic anhydrase inhibitors, or alpha-agonists
- Patients who have started or changed glucocorticoids therapy in the last 3 months
- Contraindications to beta blockers (see below)
- Any use of a non-FDA approved medication for glaucoma in the last 3 months
- Patients who smoke or have irregular daily sleep patterns
Tracking Information
- NCT #
- NCT02165631
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Malik Y Kahook, MD University of Colorado, Denver
- Malik Y Kahook, MD University of Colorado, Denver