Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis in Intraocular Pressure (IOP) After Bevacizumab
Primary Purpose
Macular Edema, Diabetic Retinopathy, Macular Degeneration
Status
Completed
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
bevacizumab
anterior chamber paracentesis
acetazolamide
brimonidine
Sponsored by
About this trial
This is an interventional trial for Macular Edema focused on measuring bevacizumab, intra-ocular pressure, acetazolamide, anterior chamber paracentesis, brimonidine, macular edema secondary to diabetic retinopathy or macular degeneration
Eligibility Criteria
Inclusion Criteria:
- macular edema
Exclusion Criteria:
- pulmonary chronic problems
- chronic renal failure
- intraocular inflammation
- drug or alcohol addiction
Sites / Locations
- School of Medicine - Clinical Hospital
Outcomes
Primary Outcome Measures
Intra-ocular pressure variation after intra-vitreous injection of bevacizumab
Secondary Outcome Measures
Full Information
NCT ID
NCT00804921
First Posted
December 8, 2008
Last Updated
December 8, 2008
Sponsor
University of Sao Paulo
1. Study Identification
Unique Protocol Identification Number
NCT00804921
Brief Title
Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis in Intraocular Pressure (IOP) After Bevacizumab
Official Title
Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis for Ocular Hypertension Control After Intravitreal Bevacizumab Injection: Preliminary Results
Study Type
Interventional
2. Study Status
Record Verification Date
December 2008
Overall Recruitment Status
Completed
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators
Name of the Sponsor
University of Sao Paulo
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Macular Edema, Diabetic Retinopathy, Macular Degeneration
Keywords
bevacizumab, intra-ocular pressure, acetazolamide, anterior chamber paracentesis, brimonidine, macular edema secondary to diabetic retinopathy or macular degeneration
7. Study Design
Study Phase
Phase 2
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
bevacizumab
Intervention Type
Procedure
Intervention Name(s)
anterior chamber paracentesis
Intervention Type
Drug
Intervention Name(s)
acetazolamide
Intervention Type
Drug
Intervention Name(s)
brimonidine
Primary Outcome Measure Information:
Title
Intra-ocular pressure variation after intra-vitreous injection of bevacizumab
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
macular edema
Exclusion Criteria:
pulmonary chronic problems
chronic renal failure
intraocular inflammation
drug or alcohol addiction
Facility Information:
Facility Name
School of Medicine - Clinical Hospital
City
Ribeirao Preto
State/Province
SP
ZIP/Postal Code
14049-900
Country
Brazil
12. IPD Sharing Statement
Learn more about this trial
Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis in Intraocular Pressure (IOP) After Bevacizumab
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