Cataract Surgery Clinical Trial
| NCT number | NCT00407017 |
| Other study ID # | 5264-T |
| Secondary ID | |
| Status | Completed |
| Phase | Phase 4 |
| First received | November 30, 2006 |
| Last updated | August 17, 2007 |
| Verified date | August 2007 |
| Source | Innovative Medical |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Interventional |
The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits.
| Status | Completed |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | |
| Gender | Both |
| Age group | N/A and older |
| Eligibility |
Inclusion Criteria: - Males or females scheduled to undergo cataract surgery - Patients can be receiving monofocal IOLs only - Likely to complete all study visits and able to provide informed consent - Visual potential of 20/25 or better Exclusion Criteria: - Known contraindications to any study medication or ingredients - Active ocular diseases or uncontrolled systemic disease - Active ocular allergies |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind
| Country | Name | City | State |
|---|---|---|---|
| United States | The Center for Excellence in Eye Care | Miami | Florida |
| Lead Sponsor | Collaborator |
|---|---|
| Innovative Medical |
United States,
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