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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00801866
Other study ID # APEC-035
Secondary ID
Status Withdrawn
Phase Phase 4
First received
Last updated
Start date December 2008
Est. completion date December 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

to evaluate the efficacy of a single intravitreal bevacizumab (IVB) injection, 0.1mL (2.5mg), against panretinal photocoagulation (PRP)-induced macular thickening and visual disturbance in patients with severe nonproliferative diabetic retinopathy (NPDR) and proliferative diabetic retinopathy (PDR) and good vision


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender All
Age group 15 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with Proliferative retinopathy or severe non-proliferative retinopathy - BCVA of 20/63 or better (56 ETDRS letters - No history of Macular Edema - Central Retinal Thickness of 250mics or more Exclusion Criteria: - Previous treatment. - Other ophthalmic diseases. history of Nephropathy, heart diseases and pregnancy - Media opacities

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bevacizumab
Intravitreal administration
Procedure:
Panretinal Photocoagulation
Panretinal Photocoagulation

Locations

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

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 Best Corrected Visual Acuity
Secondary Central Retinal Thickness.
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