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| Sponsor: | Innovative Medical |
|---|---|
| Information provided by: | Innovative Medical |
| ClinicalTrials.gov Identifier: | NCT00407017 |
Purpose
The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits.
| Condition | Intervention | Phase |
|---|---|---|
|
Cataract Surgery |
Drug: Gatifloxacin Drug: Ketorolac LS Drug: Pred Forte Drug: Moxifloxacin Drug: Nepafenac Drug: EconoPred Plus |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Randomized, Double-Blind, Active Control, Parallel Assignment |
Eligibility| Genders Eligible for Study: | Both |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Florida | |
| The Center for Excellence in Eye Care | |
| Miami, Florida, United States, 33176 | |
| Principal Investigator: | William Trattler, MD | The Center For Excellence in Eye Care |
More Information
| Study ID Numbers: | 5264-T |
| Study First Received: | November 30, 2006 |
| Last Updated: | August 17, 2007 |
| ClinicalTrials.gov Identifier: | NCT00407017 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
Anti-Inflammatory Agents Anti-Infective Agents Antineoplastic Agents Methylprednisolone Physiological Effects of Drugs Hormones, Hormone Substitutes, and Hormone Antagonists Antiemetics Prednisolone acetate Lens Diseases Neuroprotective Agents Hormones Moxifloxacin Therapeutic Uses Cataract |
Methylprednisolone Hemisuccinate Antineoplastic Agents, Hormonal Eye Diseases Gastrointestinal Agents Methylprednisolone acetate Protective Agents Glucocorticoids Pharmacologic Actions Gatifloxacin Autonomic Agents Prednisolone Peripheral Nervous System Agents Central Nervous System Agents |