CompletedPhase 2NCT01710332
The Safety & Efficacy of Intravitreal Aflibercept Injection in Patients With Persistent Central Serous Chorioretinopathy
Studying Central serous chorioretinopathy
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
- Wills Eye
- Principal Investigator
- Allen Ho, MD
- Intervention
- Intravitreal Aflibercept Injection(drug)
- Enrollment
- 12 enrolled
- Eligibility
- 18-60 years · All sexes
- Timeline
- 2012 – 2013
Study locations (2)
- Mid Atlantic Retina- Huntingdon Valley, Huntingdon Valley, Pennsylvania, United States
- Mid Atlantic Retna- Wills Eye Institute, Philadelphia, Pennsylvania, United States
Collaborators
Regeneron Pharmaceuticals
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.
Open NCT01710332 on ClinicalTrials.govOther trials for Central serous chorioretinopathy
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