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Phase 4 N=35 Randomized Double-blind Treatment

Circadian Ocular Perfusion Pressure and Ocular Blood Flow

Glaucoma

Enrolled (actual)
35
Serious AEs
1.5%
Results posted
Mar 2013
Primary outcome: Primary: Mean Change From Baseline in Overall Diastolic Ocular Perfusion Pressure at Week 6 — 2.6; 0.8 mmHg (millimeters of mercury)

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Brinzolamide 10 mg/ml/Timolol 5 mg/ml eye drops suspension (Drug); Brimonidine 20 mg/ml/Timolol 5 mg/ml eye drops solution (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Alcon Research
Primary completion
Jan 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Change From Baseline in Overall Diastolic Ocular Perfusion Pressure at Week 6
2.6; 0.8
SECONDARY
Mean Change From Baseline in Circadian Diastolic Ocular Perfusion Pressure at Week 6
2.8; 6.5; 3.0; 2.1; 4.4; 3.9
SECONDARY
Mean Change From Baseline in Mean Flow Value in the Superotemporal Peripapillary Retina at Week 6
-272.4; -43.5; -12.1; 248.9; -26.7; -51.3
SECONDARY
Mean Change From Baseline in Mean Flow Value in the Inverotemporal Peripapillary Retina at Week 6
15.9; -70.0; -40.7; -89.2; -38.7; -69.1
SECONDARY
Mean Change From Baseline in Intraocular Pressure (IOP) at Week 6
-6.3; -6.5; -6.0; -6.5; -5.6; -5.2
SECONDARY
Mean Change From Baseline in Diastolic Blood Pressure at Week 6
-3.3; 0.6; -3.5; -4.3; -1.5; -0.9
SECONDARY
Mean Change From Baseline in Systolic Blood Pressure at Week 6
-4.2; 4.5; -2.6; -1.9; -2.9; -0.4
SECONDARY
Mean Change From Baseline in Vascular Resistance in the Central Retinal Artery at Week 6
-0.00; 0.01; -0.01; 0.01; 0.00; -0.00
SECONDARY
Mean Change From Baseline in Vascular Resistance in the Ophthalmic Artery at 6 Weeks
-0.01; -0.01; 0.02; 0.02; 0.01; 0.01
SECONDARY
Mean Change From Baseline in End Diastolic Velocity in the Ophthalmic Artery at Week 6
-0.0; -0.8; -0.6; -1.2; 0.5; 0.2
SECONDARY
Mean Change From Baseline in Peak Systolic Velocity in the Ophthalmic Artery at Week 6
-1.0; -3.8; -0.7; -1.4; 2.2; 1.3
SECONDARY
Mean Change From Baseline in Peak Systolic Velocity in the Central Retinal Artery at Week 6
0.9; 0.7; -0.2; 0.3; 1.0; 0.6

Summary

The purpose of this study was to compare the short term effects of two intraocular pressure (IOP) lowering medications on ocular perfusion pressure (OPP), ocular blood flow, intraocular pressure, and blood pressure in patients with glaucoma. Ocular perfusion pressure (OPP) is defined as the difference between arterial blood pressure (diastolic and systolic) and intraocular pressure. The primary efficacy assessment is based on diastolic ocular perfusion pressure.

Eligibility Criteria

Inclusion Criteria

  • Sign Informed Consent.
  • Diagnosis of open-angle glaucoma in at least one eye.
  • Requires more than one IOP-lowering medication.
  • IOP measurements at Screening, Safety, and Eligibility/Period 1 Baseline Visits as specified in protocol.
  • Able to discontinue all IOP-lowering medication prior to Eligibility Visit and for 4 weeks between treatment periods.
  • Willing to complete all required study visits.
  • Other protocol-defined inclusion criteria may apply.

Exclusion Criteria

  • Female of child-bearing potential if pregnant, lactating, or not using highly effective birth control measures.
  • Severe central visual field loss in either eye.
  • Previous glaucoma surgery in the study eye.
  • Intraocular surgery in the study eye within 3 months prior to the Screening Visit.
  • Wears contact lenses.
  • Allergy/hypersensitivity to study medication.
  • Cannot safely discontinue use of glucocorticoid medication.
  • Uses medication that could affect IOP or blood pressure.
  • Recent use of high-dose aspirin.
  • Bronchial asthma or severe chronic obstructive pulmonary disease.
  • Diabetic retinopathy.
  • Any abnormality preventing reliable tonometry.
  • Any severe illness or condition unsuitable for the study, in the opinion of the investigator.
  • Other protocol-defined exclusion criteria may apply.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00800540). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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