Trials / Withdrawn
WithdrawnNCT02309736
OTX-14-002: Device Exposure Registry
Device Exposure Registry: A Post-Approval Observational Registry of ReSure Sealant to Track the Incidence of Endophthalmitis After Sealing Corneal Incisions in Patients Undergoing Clear Corneal Cataract Surgery
- Status
- Withdrawn
- Phase
- —
- Study type
- Observational
- Enrollment
- 0 (actual)
- Sponsor
- Ocular Therapeutix, Inc. · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ReSure Sealant |
Timeline
- Primary completion
- 2020-04-01
- First posted
- 2014-12-05
- Last updated
- 2020-02-05
Source: ClinicalTrials.gov record NCT02309736. Inclusion in this directory is not an endorsement.