Prospective Evaluation of Near and Intermediate Visual Outcomes With Monofocal Intraocular Lenses: The Mast Study

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-08-31

Study Completion Date

2012-10-31

Brief Summary

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The purpose of this study is to evaluate the near and intermediate visual outcomes of patients who have undergone routine cataract surgery (removal of cloudy crystalline lens) with phacoemulsification (the break-up and removal of cloudy lens) and monofocal IOL ( a plastic lens implanted to replace eye's natural lens) placement in the capsular bag in at least one eye.

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Detailed Description

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Conditions

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Patients Implanted With Monofocal Intraocular Lens

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Near visual outcomes with Monofocal IOL

Evaluation of intermediate visual outcomes of patients undergoing routine cataract surgery with phacoemulsification and monofocal IOl placement in the capsular bag in at least one eye.

Monofocal Intraocular Lenses

Intervention Type DEVICE

Monofocal Intraocular Lenses

Intermediate Visual outcomes

Evaluation of intermediate visual outcomes of patients undergoing routine cataract surgery with phacoemulsification and monofocal IOl placement in the capsular bag in at least one eye.

Monofocal Intraocular Lenses

Intervention Type DEVICE

Monofocal Intraocular Lenses

Interventions

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Monofocal Intraocular Lenses

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Male or female patients at least 18 years of age
* Patients who underwent routine cataract surgery with phacoemulsification and monofocal iol placement in the capsular bag in at least one eye within the last 36 months
* At least 1 month postop before follow-up evaluation
* All Patients must have a DCVA of 20/25 or better

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes