ReSure Sealant Device Exposure Registry
| Status: | Recruiting |
|---|---|
| Conditions: | Ocular |
| Therapuetic Areas: | Ophthalmology |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 2/16/2017 |
| Start Date: | January 2016 |
| End Date: | January 2019 |
| Contact: | Eric Ankerud |
| Email: | eankerud@ocutx.com |
| Phone: | 781-357-4013 |
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
This is a prospective multicenter observational single arm post-approval registry that will
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.
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.
Inclusion Criteria:
- Received at least one application of the ReSure Sealant on the operative eye
following cataract surgery
Exclusion Criteria:
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