UnknownPhase 1NCT01011374
Impact of Lucentis on Psychological Morbidity in Patients With Retinal Vein Occlusion
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
- Retina Associates of Cleveland, Inc
- Principal Investigator
- Lawrence J Singerman, MDRetina Associates of Cleveland
- Intervention
- ranibizumab (Lucentis)(drug)
- Enrollment
- 45 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2009 – 2013
Study locations (1)
- Retina Associates of Cleveland, Cleveland, Ohio, 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.
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