Suspended

Intravitreal Bevacizumab for Diabetic Macular Edema

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What is being tested

Data Collection

Who is being recruted

Cardiovascular Diseases+9

+ Diabetes Mellitus

+ Diabetic Angiopathies

See all eligibility criteria
How is the trial designed

Phase 2 & 3
Interventional
See protocol details

Summary

Principal SponsorIsfahan Ophthalmology Research Center
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Diabetic macular edema is a common cause of visual loss among diabetic patients. Studies have demonstrated the role of vascular endothelial growth factor (VEGF) in the pathogenesis of edema. This study designed to evaluate the effect of Intravitreal injection of a recombinant monoclonal anti-VEGF antibody, Bevacizumab, for treatment of diabetic macular edema.

Official TitleIntravitreal Bevacizumab for Diabetic Macular Edema
NCT00703235
Principal SponsorIsfahan Ophthalmology Research Center
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiovascular DiseasesDiabetes MellitusDiabetic AngiopathiesDiabetic RetinopathyEndocrine System DiseasesEye DiseasesMacular DegenerationMacular EdemaRetinal DegenerationRetinal DiseasesVascular DiseasesDiabetes Complications

Criteria

Inclusion Criteria: * Diabetes mellitus * Clinically significant macular edema * Possibility of performing macular OCT * Consent of patient for inclusion in the study Exclusion Criteria: * History of macular photocoagulation in less than 6 months of inclusion in the study * Necessity of surgical intervention * Rejection of the remaining in the study by patient

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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