Status:
WITHDRAWN
OTX-14-002: Device Exposure Registry
Lead Sponsor:
Ocular Therapeutix, Inc.
Conditions:
Endophthalmitis
Eligibility:
All Genders
Brief 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...
Eligibility Criteria
Inclusion
- All patients that receive at least one application of the ReSure Sealant on the operative eye following cataract surgery will be enrolled.
Exclusion
Key Trial Info
Start Date :
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT02309736
Last Update
February 5 2020
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