Therapeutic Variables in Cataract Surgery
Sponsor
Innovative Medical (Industry)
Overall Status
Completed
CT.gov ID
NCT00407017
Collaborator
(none)
1
Study Details
Study Description
Brief Summary
The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Study Design
Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
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
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Center for Excellence in Eye Care | Miami | Florida | United States | 33176 |
Sponsors and Collaborators
- Innovative Medical
Investigators
- Principal Investigator: William Trattler, MD, The Center For Excellence in Eye Care
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00407017
Other Study ID Numbers:
- 5264-T
First Posted:
Dec 4, 2006
Last Update Posted:
Aug 21, 2007
Last Verified:
Aug 1, 2007
Additional relevant MeSH terms: