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NCT00804206 Clinical Trial

Comparison of the Effects of Bevacizumab Before vs After Pattern Panretinal Photocoagulation

Macular Edema Clinical Trial

Official title:
Phase 4 Comparison of the Effects of Bevacizumab Before vs After Pattern Panretinal Photocoagulation

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00804206
Other study ID # APEC-040
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date July 2008
Est. completion date July 2008

Study information
Verified date May 2024
Source Asociación para Evitar la Ceguera en México
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare the effect of an intravitreal injection of bevacizumab previous or posterior of panretinal laser photocoagulation (PRLP) with a pattern laser; to prevent and reduce diabetic macular edema (DME) in patients with proliferative diabetic retinopathy (PDR) with DME.

Recruitment information / eligibility
Status Terminated
Enrollment 15
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers No
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - Patients with proliferative diabetic retinopathy - patients with macular edema Exclusion Criteria: - patients with previous treatments - patients with ocular surgeries

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• bevacizumab
Intravitreal bevacizumab before panretinal photocoagulation
• bevacizumab
Intravitreal Bevacizumab after panretinal photocoagulation

Locations
Country Name City State
Mexico Asociación para Evitar la Ceguera en México México

Sponsors (1)
Lead Sponsor Collaborator
Asociación para Evitar la Ceguera en México

Country where clinical trial is conducted

Mexico, 

Outcome
Type Measure Description Time frame Safety issue
Primary Central macular thickness baseline, 10 days, 52 days, 85 days
Secondary Best corrected visual acuity baseline, 10 days, 52 days, 85 days
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