Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis in Intraocular Pressure (IOP) After Bevacizumab
NCT ID: NCT00804921
Last Updated: 2008-12-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
INTERVENTIONAL
Brief Summary
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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.
Detailed Description
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Conditions
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Keywords
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Interventions
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bevacizumab
anterior chamber paracentesis
acetazolamide
brimonidine
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* chronic renal failure
* intraocular inflammation
* drug or alcohol addiction
50 Years
ALL
No
Sponsors
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University of Sao Paulo
OTHER
Locations
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School of Medicine - Clinical Hospital
Ribeirão Preto, São Paulo, Brazil
Countries
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Other Identifiers
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IOP After Bevacizumab
Identifier Type: -
Identifier Source: org_study_id