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Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis for Ocular Hypertension Control After Intravitreal Bevacizumab

Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis for Ocular Hypertension Control After Intravitreal Bevacizumab Injection

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00864838
Enrollment
56
Registered
2009-03-19
Start date
2008-06-30
Completion date
2009-03-31
Last updated
2009-03-19

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

Conditions

Age Related Macular Degeneration, Diabetic Retinopathy

Keywords

intraocular pressure, bevacizumab, acetazolamide, brimonidine, anterior chamber paracentesis

Brief summary

The purpose of this study is to evaluate the effects of anterior chamber paracentesis, brimonidine and oral acetazolamide to reduce intra-ocular pressure variations after intravitreal bevacizumab injection.

Interventions

DRUGAcetazolamide

250 mg 1 hour before intravitreal injection

DRUGBrimonidine tartarate

1 drop 1 hour before intravitreal injection

Immediately after bevacizumab injection

Sponsors

Fundação de Apoio ao Ensino Pesquisa e Assitência do HCFMRPUSP
CollaboratorUNKNOWN
University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Diagnosis of age related macular disease or diabetic retinopathy * Able and willing to provide informed consent

Exclusion criteria

* History of ocular hypertension or glaucoma * High Myopes (\> 6 spherical diopters) * High Hyperopes (\> 4 spherical diopters) * Pulmonary disease * Renal disease * Known allergy to any component of the study drug * Myocardial infarction, transient ischemic attack within 4 months prior to randomization or any contraindication for bevacizumab use

Design outcomes

Primary

MeasureTime frame
Intraocular pressure (mmHg)1 hour and, 3 minutes before IVI. 3,10,20, 30 minutes after IVI

Outcome results

None listed

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