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Completed Phase 3 Interventional Results available

DRCR.Net Aflibercept vs. Bevacizumab + Deferred Aflibercept for the Treatment of CI-DME

ClinicalTrials.gov ID: NCT03321513

Public ClinicalTrials.gov record NCT03321513. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized Trial of Intravitreous Aflibercept Versus Intravitreous Bevacizumab + Deferred Aflibercept for Treatment of Central-Involved Diabetic Macular Edema

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Both aflibercept and bevacizumab have been shown to improve vision in eyes with DME. In eyes with DME and at least moderate vision loss, both aflibercept and bevacizumab were also shown to be successful in many eyes. However, aflibercept was shown to be more effective at improving vision, on average, at 1 year and at 2 years. Due to the large cost difference between the two drugs, many clinicians and patients are choosing to initiate treatment with bevacizumab and then switch to aflibercept depending on the eye's response to bevacizumab treatment. However, there is no scientific evidence that this treatment strategy is as effective at improving vision as initiating treatment with aflibercept. Patients and clinicians do not know if this approach ultimately has deleterious effects on visual acuity. If starting with aflibercept is not better than starting with bevacizumab and switching to aflibercept if needed, the potential cost savings to future patients and the health care system would be substantial. However, if starting with aflibercept is better, then patients, clinicians, and health care providers can make informed decisions for how to best treat patients with DME and at least moderate vision loss. Study Objectives To compare the efficacy of intravitreous aflibercept with intravitreous bevacizumab + deferred aflibercept if needed in eyes with CI DME and moderate vision loss

Study identification

NCT ID
NCT03321513
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
270 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 7, 2017 (Actual)
Primary completion
Dec 22, 2021 (Actual)
Completion
Dec 22, 2021 (Actual)
Last update posted
Oct 1, 2026

2017 – 2021

United States locations

U.S. sites
54
U.S. states
23
U.S. cities
49
Facility City State ZIP Site status
Retinal Diagnostic Center Campbell California 95008 —
Macula & Retina Institute Glendale California 91203 —
Loma Linda University Health Care, Department of Ophthalmology Loma Linda California 92354 —
East Bay Retina Consultants, Inc Oakland California 94609-3028 —
National Ophthalmic Research Institute Fort Myers Florida 33912 —
Florida Retina Institute-Jacksonville Jacksonville Florida 32216 —
Florida Retina Consultants Lakeland Florida 33805 —
Retina Macula Specialists of Miami Miami Florida 33126 —
Central Florida Retina Orlando Florida 32806 —
Florida Retina Institute Orlando Florida 32806 —
Southeast Eye Institute, P.A. dba Eye Associates of Pinellas Pinellas Park Florida 33782 —
Fort Lauderdale Eye Institute Plantation Florida 33324 —
Retina Associates of Sarasota Sarasota Florida 34233 —
Sarasota Retina Institute Sarasota Florida 34239 —
Retina Associates of Florida, LLC Tampa Florida 33609 —
Retina Specialists of Tampa Wesley Chapel Florida 33544 —
Southeast Retina Center, P.C. Augusta Georgia 30909 —
Thomas Eye Group Sandy Springs Georgia 30328 —
Illinois Retina Associates, S.C. Oak Park Illinois 60304 —
Springfield Clinic, LLP Springfield Illinois 62703 —
Raj K. Maturi, M.D., P.C. Indianapolis Indiana 46290 —
John-Kenyon American Eye Institute New Albany Indiana 47150 —
Mid-America Retina Consultants, P.A. Overland Park Kansas 66211 —
Retina Associates, P.A. Shawnee Mission Kansas 66204 —
Paducah Retinal Center Paducah Kentucky 42001 —
Eye Associates of Northeast Louisiana dba Haik Humble Eye Center West Monroe Louisiana 71291 —
Mid Atlantic Retina Specialists Hagerstown Maryland 21740 —
Valley Eye Physicians and Surgeons Ayer Massachusetts 01432 —
Joslin Diabetes Center Boston Massachusetts 02215 —
Retina Specialists of Michigan Grand Rapids Michigan 49546 —
Vitreo-Retinal Associates Grand Rapids Michigan 49546 —
The Retina Institute St Louis Missouri 63128 —
Eye Associates of New Mexico Albuquerque New Mexico 87109 —
MaculaCare New York New York 10021 —
Retina Associates of Western New York Rochester New York 14620 —
Western Carolina Clinical Research, LLC Asheville North Carolina 28803 —
Charlotte Eye, Ear, Nose and Throat Assoc., PA Charlotte North Carolina 28210 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Dean A. McGee Eye Institute Oklahoma City Oklahoma 73104 —
Retina Northwest, PC Portland Oregon 97221 —
Cascade Medical Research Institute, LLC Springfield Oregon 97477 —
Retina Vitreous Consultants Monroeville Pennsylvania 15146 —
Retinavitreous Associates, dba; Mid Atlantic Retina Philadelphia Pennsylvania 19107-5109 —
Southeastern Retina Associates, P.C. Knoxville Tennessee 37909 —
Austin Retina Associates Austin Texas 78705 —
Retina Research Center Austin Texas 78705 —
Retina Center of Texas Grapevine Texas 76051 —
Baylor Eye Physicians and Surgeons Houston Texas 77030 —
Retina Consultants of Houston, PA Houston Texas 77030 —
Texas Retina Associates Lubbock Texas 79424 —
Valley Retina Institute McAllen Texas 78503 —
Retinal Consultants of San Antonio San Antonio Texas 78240 —
Spokane Eye Clinic Spokane Washington 99204 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03321513, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 1, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03321513 live on ClinicalTrials.gov.

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