CompletedPhase 2NCT02354170
Short-Term Oral Mifepristone for 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
- Roger Goldberg, M.D., MBA
- Principal Investigator
- Roger A Goldberg, M.D., MBA, MDBay Area Retina Associates
- Intervention
- Mifepristone(drug)
- Enrollment
- 16 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2015 – 2017
Study locations (2)
- Bay Area Retina Associates, Walnut Creek, California, United States
- Ophthalmic Consultants of Boston, Boston, Massachusetts, United States
Collaborators
Ophthalmic Consultants of Boston
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 NCT02354170 on ClinicalTrials.govOther trials for Central serous chorioretinopathy
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