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NCT00349583 Clinical Trial

Efficacy of Topical Cyclosporine Versus Tears for Improving Visual Outcomes Following Multifocal IOL Implantation

Cataract Clinical Trial

Official title:
Efficacy of Topical Cyclosporine Versus Tears for Improving Visual Outcomes Following Multifocal IOL Implantation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00349583
Other study ID # 1683
Secondary ID
Status Completed
Phase Phase 4
First received July 5, 2006
Last updated May 30, 2007

Study information
Verified date May 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 evaluate the efficacy on quality of vision and dry eye signs and symptoms in patients undergoing cataract surgery using the ReZoom® multifocal IOL.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

- · Males or females > 50 years old

- Scheduled to undergo bilateral phacoemulsification with implantation of a multifocal IOL.

- Likely to complete all study visits and able to provide informed consent

- Visual potential of 20/25 or better

Exclusion Criteria:

- · Prior use of topical cyclosporine

- 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:
• Topical Cyclosporine, Tears

Locations
Country Name City State
United States Ophthalmic Consultants of Long Island Rockville Centre New York

Sponsors (1)
Lead Sponsor Collaborator
Innovative Medical

Country where clinical trial is conducted

United States, 

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