OTX-14-002: Device Exposure Registry
NCT02309736 · Status: WITHDRAWN · Type: OBSERVATIONAL
Last updated 2020-02-05
Summary
The objective of the study is to collect post-approval data relative to the incidence of endophthalmitis for cataract surgery patients treated with the FDA-approved ReSure Sealant when used by a broad group of physicians under commercial use conditions
Conditions
- Endophthalmitis
Interventions
- DEVICE
-
ReSure Sealant
Sponsors & Collaborators
-
Ocular Therapeutix, Inc.
lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Primary Completion
- 2020-04-30
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