Vitrectomy Clinical Trial
| NCT number | NCT00377546 |
| Other study ID # | 5264 |
| Secondary ID | |
| Status | Completed |
| Phase | Phase 4 |
| First received | September 14, 2006 |
| Last updated | September 23, 2008 |
| Verified date | September 2008 |
| Source | Innovative Medical |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Interventional |
To compare the penetration of three different NSAIDs.
| 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 Vitrectomy surgery - 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 | Ophthalmic Consultants of Boston | Boston | Massachusetts |
| Lead Sponsor | Collaborator |
|---|---|
| Innovative Medical |
United States,
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT04409808 -
IRIS Alfa Clinical Trial A Monocentric, Academic Clinical Trial Safety Study of a Prototype of a New Vitrectomy Device.
|
N/A | |
| Active, not recruiting |
NCT04566237 -
Objective Measurements of the Opacification of the Lens After Vitrectomy
|
N/A | |
| Completed |
NCT00532415 -
Safety and Efficacy of Vitreous Delineating Agent During Vitrectomy
|
Phase 3 | |
| Completed |
NCT04076072 -
Beveled-Tip Versus(vs) Standard-Tip Vitrectomy Probe
|
N/A | |
| Not yet recruiting |
NCT03633266 -
Anti-VEGF Instead of Intraoperative PRP in Proliferative Diabetic Retinopathy
|
N/A | |
| Completed |
NCT00927628 -
Macular Hole Reopening
|
N/A | |
| Not yet recruiting |
NCT03637283 -
Anti-VEGF Instead of Intraoperative Fan-shaped Photocoagulation in BRVO Combined With Vitreous Hemorrhage
|
N/A | |
| Completed |
NCT01255293 -
Comparative Study of 1000 Centistoke Versus 5000 Centistoke Silicone Oil for Repair of Complex Retinal Detachments
|
N/A | |
| Terminated |
NCT01023009 -
Postoperative Evolution After Small Gauge Vitrectomy Without Eye Occlusion
|
||
| Completed |
NCT00737022 -
Macular Appearance After Diabetic Vitrectomy
|
N/A | |
| Completed |
NCT03902795 -
Functional and Morphological Results of Rhegmatogenous Retinal Detachment Treated With Vitrectomy
|
||
| Completed |
NCT02644694 -
PK Study of Iontophoretic Dexamethasone Phosphate Ophthalmic Solution in Patients Undergoing Vitrectomy
|
Phase 1 | |
| Completed |
NCT01319318 -
Observational Study of Ocular Inflammation in Patients Undergoing a Pars Plana Vitrectomy
|
N/A | |
| Not yet recruiting |
NCT04346095 -
Oral Sedation in Vitreoretinal Surgery
|
Phase 4 | |
| Completed |
NCT01159665 -
The Purpose of This Study is to Evaluate the Pharmacokinetic Properties of Intravitreal Ocriplasmin Prior to Planned Primary Pars Plana Vitrectomy (PPV)
|
Phase 2 | |
| Completed |
NCT00685490 -
Vitrectomy for Branch Retinal Vein Occlusion
|
N/A | |
| Completed |
NCT05446948 -
Observation of the Efficacy of Different Vitrectomy Systems to Treat Proliferative Diabetic Retinopathy
|
N/A | |
| Completed |
NCT05710458 -
Performance Comparison of the 25 Gauge 20,000cpm HYPERVIT Dual Blade vs. 10,000cpm ULTRAVIT Vitrectomy Cutter
|
N/A | |
| Terminated |
NCT02995746 -
Intravitreal Dexamethasone Implant for Persistent Macular Thickening and Edema After Vitrectomy for Epiretinal Membrane
|
N/A | |
| Completed |
NCT03701542 -
The Application of M-charts and Microperimetry for the Assessment of Visual Function in Patients After Vitrectomy Due to the Full Thickness Macular Hole.
|