A Continuation Study To Monitor The Long Term Safety Of Patients Completing Protocols ACU-P08-020/020A

Completed · Not applicable

Conditions studied: Presbyopia

In brief

This is a 2 year follow up study to monitor the long term safety of the ACI 7000PDT in subjects who are still implanted with the ACI and have successfully completed the ACU-P08-020/020A studies.

Key facts

Study ID

NCT01895088

Run by

AcuFocus, Inc.

People needed

271

Starts

2011-05-01

Expected to finish

2015-08-01

Last updated by the study team

2017-08-01

Who can join

Age: 45 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients must have completed participation in the ACU-P08-020/020A clinical trial.
• Patients must be able to provide voluntary informed consent, and must sign and be given a copy of the written Informed Consent form.

You may not qualify if…

• Patients who did not complete ACU-P08-020/020A.

Where it is running

• McDonald Eye Associates — Fayetteville, Arkansas, United States
• Maloney Vision — Los Angeles, California, United States
• NVision — Newport Beach, California, United States
• Eye Center NOCO — Fort Collins, Colorado, United States
• Kraff Eye Institute — Chicago, Illinois, United States
• Eye Surgeons of Indiana — Indianapolis, Indiana, United States
• Durrie Vision — Overland Park, Kansas, United States
• Pepose Vision Institute — Chesterfield, Missouri, United States
• The Cornea & Laser Eye Institute, P.A — Teaneck, New Jersey, United States
• University of Rochester Eye Institute - Strong Vision — Rochester, New York, United States
• Vance Thompson Vision — Sioux Falls, South Dakota, United States
• Hoopes Vision — Sandy City, Utah, United States
• Davis Duehr Dean — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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