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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00407017
Other study ID # 5264-T
Secondary ID
Status Completed
Phase Phase 4
First received November 30, 2006
Last updated August 17, 2007

Study information

Verified date August 2007
Source Innovative Medical
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits.


Recruitment information / eligibility

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 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

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind


Related Conditions & MeSH terms


Intervention

Drug:
Gatifloxacin

Ketorolac LS

Pred Forte

Moxifloxacin

Nepafenac

EconoPred Plus


Locations

Country Name City State
United States The Center for Excellence in Eye Care Miami Florida

Sponsors (1)

Lead Sponsor Collaborator
Innovative Medical

Country where clinical trial is conducted

United States, 

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