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Completed Not applicable Interventional Accepts healthy volunteers

Safety and Effectiveness Study of the AcuFocus Corneal Inlay ACI 7000PDT in Presbyopes

ClinicalTrials.gov ID: NCT00819299

Public ClinicalTrials.gov record NCT00819299. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 7, 2026, 7:24 AM EST

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Official title

A Prospective, Multicenter Clinical Trial to Evaluate the Safety and Effectiveness of the AcuFocus Corneal Inlay (ACI)™ ACI 7000PDT in Presbyopic Subjects

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine if the AcuFocus Corneal Inlay ACI 7000PDT will provide an effective method for the correction of presbyopia in patients who have normal distance vision but need a correction such as glasses or contact lenses to see clearly at near.

Study identification

NCT ID
NCT00819299
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
AcuFocus, Inc.
Industry
Enrollment
359 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
45 Years to 60 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2008 (Type not available)
Primary completion
Sep 2013 (Actual)
Completion
Sep 2013 (Actual)
Last update posted
Feb 5, 2018

2008 – 2013

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
McDonald Eye Associates Fayetteville Arkansas 72703 —
Maloney Vision Los Angeles California 90024 —
TLC Laser Eye Center Newport Beach California 92660 —
Gordon Binder Weiss Vision Institute San Diego California 92122 —
Eye Center NOCO Fort Collins Colorado 80525 —
Kraff Eye Institute Chicago Illinois 60602 —
Eye Surgeons of Indiana Indianapolis Indiana 46256 —
Durrie Vision Overland Park Kansas 66211 —
Pepose Vision Institute Chesterfield Missouri 63017 —
The Cornea & Laser Eye Institute, P.A Teaneck New Jersey 07666 —
Coleman Vision Albuquerque New Mexico 87109 —
University of Rochester Eye Institute - Strong Vision Rochester New York 14618 —
Vance Thompson Vision Sioux Falls South Dakota 57105 —
Hoopes Vision Sandy City Utah 84070 —
Davis Duehr Dean Madison Wisconsin 53715 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00819299, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 5, 2018 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00819299 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →