CompletedPhase 1NCT00403325
Intravitreal Ranibizumab Treatment of 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
- Vitreous -Retina- Macula Consultants of New York
- Principal Investigator
- Richard F. Spaide, M.D.Vitreous Retina Macula Consultants of New York, P.C.
- Intervention
- rhuFab V2 [ranibizumab] ( Lucentis )(drug)
- Enrollment
- 9 enrolled
- Eligibility
- All sexes
- Timeline
- 2006
Study locations (1)
- Vitreous Retina Macula Consultants of New York, P.C., New York, New York, United States
Collaborators
Genentech, Inc.
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 NCT00403325 on ClinicalTrials.govOther trials for Central serous chorioretinopathy
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