CompletedPhase 2NCT03126786
Suprachoroidal CLS-TA With Intravitreal Aflibercept Versus Aflibercept Alone in Subject With Diabetic Macular Edema
Studying Central retinal vein occlusion
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Clearside Biomedical, Inc.
- Principal Investigator
- Thomas Ciulla, MDClearside Biomedical
- Intervention
- IVT aflibercept(drug)
- Enrollment
- 71 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2018
Study locations (29)
- Retinal Consultants of Arizona and Retinal Research Institute, Phoenix, Arizona, United States
- Retina Centers, PC, Tucson, Arizona, United States
- California Retina Consultants, Bakersfield, California, United States
- Retina Vitreous Medical Group Clinical Research, Beverly Hills, California, United States
- Northern California Retina Vitreous Associates Medical Group, Inc., Mountain View, California, United States
- Retina Institute of California, Palm Desert, California, United States
- Retina Consultants San Diego, Poway, California, United States
- MedEye Associates, Miami, Florida, United States
- Retina Specialty Institute, Pensacola, Florida, United States
- Sarasota Retina Institute, Sarasota, Florida, United States
- Center for Retina and Macular Disease, Winter Haven, Florida, United States
- Emory Eye Center, Augusta, Georgia, United States
- Marietta Eye Clinic, Marietta, Georgia, United States
- Midwest Eye Institute, Indianapolis, Indiana, United States
- Retina and Vitrous Associates of Kentucky, Lexington, Kentucky, United States
- +14 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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