Therapeutic Variables in Cataract Surgery
The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits...
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.
- Study Type: Interventional
- Study Design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind
Intervention(s) in this Clinical Trial
- Drug: Gatifloxacin
- Drug: Ketorolac LS
- Drug: Pred Forte
- Drug: Moxifloxacin
- Drug: Nepafenac
- Drug: EconoPred Plus
Criteria for Participation in this Clinical Trial
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
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: N/A
Maximum Age for this Clinical Trial: N/A
Clinical Trial Investigator Information
Lead Investigator: Innovative Medical Industry
Overall Clinical Trial Officials and Contacts
William Trattler, MD Principal Investigator The Center For Excellence in Eye Care
Additional Information
Information obtained from ClinicalTrials.gov on February 12, 2012
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00407017
Study ID Number: 5264-T
ClinicalTrials.gov Identifier: NCT00407017
Health Authority: United States: Institutional Review Board
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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00407017
