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

Information source: University of Sao Paulo
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Age Related Macular Degeneration; Diabetic Retinopathy

Intervention: Acetazolamide (Drug); Brimonidine tartarate (Drug); Anterior chamber paracentesis (Procedure)

Phase: Phase 2

Status: Completed

Sponsored by: University of Sao Paulo

Official(s) and/or principal investigator(s):
Rodrigo Jorge, MD, Study Chair, Affiliation: University of São Paulo
Marco A Bonini-Filho, MD, Principal Investigator, Affiliation: University of São Paulo
Bianka Y Katayama, MD, Study Director, Affiliation: Clinic´s Hospital, Ribeirão Preto Medical School, University of São Paulo

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.

Clinical Details

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

Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Primary outcome: Intraocular pressure (mmHg)

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

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

Locations and Contacts

Additional Information

Starting date: June 2008
Last updated: March 18, 2009

Page last updated: August 20, 2015

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