Clinical Trials Directory

Trials / Completed

CompletedNCT00804921

Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis in Intraocular Pressure (IOP) After Bevacizumab

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

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
University of Sao Paulo · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

Purpose: To evaluate the effects of anterior chamber paracentesis, brimonidine and oral acetazolamide to reduce intra-ocular pressure (IOP) variations after intravitreal bevacizumab injection (IVBV). Methods: 47 patients scheduled for IVBV (1.5 mg / 0.06 ml) will be randomly assigned to a pre-treatment 1 hour before IVBV with either 250 mg oral acetazolamide (DIA, 9 eyes), anterior chamber paracentesis immediate after IVBV (PAR, 15 eyes), topic brimonidine tartarate 1 hour before IVBV (BRI, 14 eyes), or no pre-treatment IBVB (CTR, 9 eyes). IOP will be measured 90 minutes before injection (baseline), just before injection, and at 3, 10, 20 and 30 minutes after the procedure.

Conditions

Interventions

TypeNameDescription
DRUGbevacizumab
PROCEDUREanterior chamber paracentesis
DRUGacetazolamide
DRUGbrimonidine

Timeline

First posted
2008-12-09
Last updated
2008-12-09

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00804921. Inclusion in this directory is not an endorsement.