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Visual Function Changes After Intraocular Pressure Reduction

Visual Function Changes After Intraocular Pressure Reduction Using Antiglaucoma Medications: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00435058
Enrollment
54
Registered
2007-02-14
Start date
2005-09-30
Completion date
2006-04-30
Last updated
2007-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma

Keywords

intraocular pressure, contrast sensitivity, visual function

Brief summary

During the glaucomatous disease process, subpopulations of cells may be dead, damaged or healthy. Visual function changes could be observed due to a recovering of the suffering ganglion cells after the intraocular pressure reduction. This study aims at evaluating the correlation between intraocular pressure reduction and visual function changes in glaucoma patients after using antiglaucoma medications.

Detailed description

Primary open angle glaucoma patients without use of antiglaucoma medications will be enrolled in this study. After inclusion, the patients will randomly receive one of three antiglaucoma medications (timolol maleate 0,5%, brimonidine tartrate 0,2% or travoprost 0,004%) in one randomly selected eye. The patients will be evaluated with Goldmann applanation tonometry, visual acuity test, contrast sensitivity test, visual quality perception test (visual analogue scale) and standard automated perimetry before and after 4 weeks of glaucoma treatment onset.

Interventions

DRUGtimolol maleate 0,5%
DRUGbrimonidine tartrate 0,2%
DRUGtravoprost 0,004%

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Primary open angle glaucoma * Intraocular pressure greater than 21 mmHg

Exclusion criteria

* Best corrected visual acuity (BCVA) worse than 20/80 * Significant media opacity * History of steroid use

Design outcomes

Primary

MeasureTime frame
intraocular pressure
contrast sensitivity
visual quality perception

Secondary

MeasureTime frame
Mean deviation of the visual field (MD)
Pattern Standard Deviation of the visual field (PSD)
visual acuity

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026