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

Sponsor
University of Sao Paulo (Other)
Overall Status
Completed
CT.gov ID
NCT00804921
Collaborator
(none)
1

Study Details

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.

Condition or Disease Intervention/Treatment Phase
Phase 2

Study Design

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

Outcome Measures

Primary Outcome Measures

  1. Intra-ocular pressure variation after intra-vitreous injection of bevacizumab []

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • macular edema
Exclusion Criteria:
  • pulmonary chronic problems

  • chronic renal failure

  • intraocular inflammation

  • drug or alcohol addiction

Contacts and Locations

Locations

Site City State Country Postal Code
1 School of Medicine - Clinical Hospital Ribeirao Preto SP Brazil 14049-900

Sponsors and Collaborators

  • University of Sao Paulo

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00804921
Other Study ID Numbers:
  • IOP After Bevacizumab
First Posted:
Dec 9, 2008
Last Update Posted:
Dec 9, 2008
Last Verified:
Dec 1, 2008

Study Results

No Results Posted as of Dec 9, 2008