Clinical trial
Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage
NCT00198497 · Bausch & Lomb Incorporated, Industry · Completed
Key facts
| NCT number | NCT00198497 |
|---|---|
| Title | Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage |
| Official title | Phase III Safety and Efficacy Study of Vitrase (Ovine Hyaluronidase) for Ophthalmic Intravitreal Injection for Clearance of Severe Vitreous Hemorrhage |
| Lead sponsor | Bausch & Lomb Incorporated, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Vitreous Hemorrhage, Diabetic Retinopathy |
| Intervention type | Drug |
| Interventions | Placebo, Vitrase |
| Enrollment | 510 |
| Start date | Jun 1, 1999 |
| Primary completion | Sep 1, 2001 |
| Completion | Jun 1, 2003 |
| First posted | Sep 20, 2005 |
| Last update posted | Mar 15, 2013 |
| Countries | Australia, Brazil, Hungary, Italy, Netherlands, Poland, South Africa, Spain, United Kingdom |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: