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

> **NCT00850031** · NA · COMPLETED · sponsor: **AcuFocus, Inc.** · enrollment: 119 (actual)

## Conditions studied

- Presbyopia

## Interventions

- **DEVICE:** AcuFocus Corneal Inlay

## Key facts

- **NCT ID:** NCT00850031
- **Lead sponsor:** AcuFocus, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2009-01
- **Primary completion:** 2013-10
- **Final completion:** 2013-10
- **Target enrollment:** 119 (ACTUAL)
- **Last updated:** 2018-02-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00850031

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00850031, "Safety and Effectiveness Study of the AcuFocus Corneal Inlay ACI 7000PDT in Presbyopes". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT00850031. Licensed CC0.

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