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Completed Not applicable Interventional Accepts healthy volunteers Results available

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

ClinicalTrials.gov ID: NCT01895088

Public ClinicalTrials.gov record NCT01895088. 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 Oct 19, 2026, 4:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Continuation Study To Monitor The Long Term Safety Of The AcuFocus ™ ACI 7000PDT Patients Completing Protocols ACU-P08-020/020A

Brief summary

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

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.

Study identification

NCT ID
NCT01895088
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
AcuFocus, Inc.
Industry
Enrollment
271 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
May 2011 (Type not available)
Primary completion
Apr 2015 (Actual)
Completion
Aug 2015 (Actual)
Last update posted
Aug 1, 2017

2011 – 2015

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
McDonald Eye Associates Fayetteville Arkansas 72703 —
Maloney Vision Los Angeles California 90024 —
NVision Newport Beach California 92660 —
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 —
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 NCT01895088, 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 Aug 1, 2017 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01895088 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →