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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01191515
Enrollment
200
Registered
2010-08-30
Start date
2010-08-31
Completion date
2012-10-31
Last updated
2012-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients Implanted With Monofocal Intraocular Lens

Keywords

Previous Cataract patients, Monofocal IOL implant, Evaluation

Brief summary

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.

Interventions

DEVICEMonofocal Intraocular Lenses

Monofocal Intraocular Lenses

Sponsors

Staar Surgical Company
CollaboratorINDUSTRY
Innovative Medical
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Countries

United States

Contacts

Primary ContactJennifer Piel
j.piel@imedsonline.com(951)653-5566

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026