CompletedPHASE1, PHASE2NCT01789320
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Studying Anterior uveitis
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, Inc.
- Intervention
- triamcinolone acetonide (Triesence®)(drug)
- Enrollment
- 11 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2013 – 2015
Study locations (3)
- Northwestern University, Chicago, Illinois, United States
- University of Nebraska Medical Center, Omaha, Nebraska, United States
- Cleveland Clinic Foundation, Cleveland, Ohio, United States
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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