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Clinical Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL)

Primary Purpose

Aphakia

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
FluidVision AIOL
Cataract Surgery
Sponsored by
PowerVision
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Aphakia focused on measuring Cataract

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Key Inclusion Criteria:

  • Eligible for primary intraocular lens implantation for the correction of aphakia following cataract extraction;
  • Best corrected distance visual acuity worse than 20/40 either with or without a glare source present (e.g. Brightness Acuity Tester);
  • Less than or equal to 1.0 diopter (D) of preoperative keratometric astigmatism;
  • Willing and able to comply with schedule for follow-up visits for 36 months after surgery.
  • Other protocol-defined inclusion criteria may apply.

Key Exclusion Criteria:

  • Systemic disease that could increase the operative risk or confound the outcome (e.g. autoimmune disease, diabetes);
  • Taking systemic medications that may confound the outcome or increase the risk to the subject;
  • Ocular conditions that may predispose for future complications;
  • Previous intraocular or corneal surgery that might confound the outcome of the investigation or increase the risk to the subject;
  • Pregnant, lactating during the course of the investigation, or with another condition associated with fluctuation of hormones that could lead to refractive changes;
  • Diagnosed degenerative visual disorders (e.g. macular degeneration or other retinal disorders) that are predicted to cause future best corrected visual acuity loss worse than 20/40.
  • Other protocol-defined exclusion criteria may apply.

Sites / Locations

  • PowerVision Investigative Site
  • PowerVision Investigative Site
  • PowerVision Investigative Site
  • PowerVision Investigative Site
  • PowerVision Investigative Site
  • PowerVision Investigative Site
  • PowerVision Investigative Site
  • PowerVision Investigative Site

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FluidVision

Arm Description

FluidVision AIOL implanted in the capsular bag of the eye during cataract surgery

Outcomes

Primary Outcome Measures

Accommodative amplitude
Accommodative amplitude is a measure of the ability of the eye to focus from a target that is at distance into a target that is near.
Best corrected distance visual acuity (BCDVA)
Visual acuity of the eye will be tested with the correction in place.
Rates of adverse events
Adverse events will be collected from time of enrollment to study exit

Secondary Outcome Measures

Full Information

First Posted
January 28, 2014
Last Updated
May 18, 2021
Sponsor
PowerVision
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1. Study Identification

Unique Protocol Identification Number
NCT02049567
Brief Title
Clinical Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL)
Official Title
Clinical Evaluation of the FluidVision Accommodating Intraocular Lens
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
January 14, 2014 (Actual)
Primary Completion Date
June 24, 2015 (Actual)
Study Completion Date
November 6, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
PowerVision

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety and effectiveness of an investigational IOL.
Detailed Description
Eligible subjects will receive the investigational IOL in one eye and be followed at 1 day, 1 week, 1 month, 3 months, 6 months, 12 months, 18 months, 24 months and 36 months post-operation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aphakia
Keywords
Cataract

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
170 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FluidVision
Arm Type
Experimental
Arm Description
FluidVision AIOL implanted in the capsular bag of the eye during cataract surgery
Intervention Type
Device
Intervention Name(s)
FluidVision AIOL
Intervention Description
Investigational implantable medical device intended for long-term use over the lifetime of the cataract subject
Intervention Type
Procedure
Intervention Name(s)
Cataract Surgery
Intervention Description
Performed using standard microsurgical techniques
Primary Outcome Measure Information:
Title
Accommodative amplitude
Description
Accommodative amplitude is a measure of the ability of the eye to focus from a target that is at distance into a target that is near.
Time Frame
Month 6
Title
Best corrected distance visual acuity (BCDVA)
Description
Visual acuity of the eye will be tested with the correction in place.
Time Frame
Month 6
Title
Rates of adverse events
Description
Adverse events will be collected from time of enrollment to study exit
Time Frame
Up to Month 36

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: Eligible for primary intraocular lens implantation for the correction of aphakia following cataract extraction; Best corrected distance visual acuity worse than 20/40 either with or without a glare source present (e.g. Brightness Acuity Tester); Less than or equal to 1.0 diopter (D) of preoperative keratometric astigmatism; Willing and able to comply with schedule for follow-up visits for 36 months after surgery. Other protocol-defined inclusion criteria may apply. Key Exclusion Criteria: Systemic disease that could increase the operative risk or confound the outcome (e.g. autoimmune disease, diabetes); Taking systemic medications that may confound the outcome or increase the risk to the subject; Ocular conditions that may predispose for future complications; Previous intraocular or corneal surgery that might confound the outcome of the investigation or increase the risk to the subject; Pregnant, lactating during the course of the investigation, or with another condition associated with fluctuation of hormones that could lead to refractive changes; Diagnosed degenerative visual disorders (e.g. macular degeneration or other retinal disorders) that are predicted to cause future best corrected visual acuity loss worse than 20/40. Other protocol-defined exclusion criteria may apply.
Facility Information:
Facility Name
PowerVision Investigative Site
City
Heidelberg
State/Province
Baden-Württemberg
ZIP/Postal Code
D-69120
Country
Germany
Facility Name
PowerVision Investigative Site
City
Stuttgart
State/Province
Baden-Württemberg
ZIP/Postal Code
D-70176
Country
Germany
Facility Name
PowerVision Investigative Site
City
Bochum
State/Province
North Rhine-Westphalia
ZIP/Postal Code
44892
Country
Germany
Facility Name
PowerVision Investigative Site
City
Berlin
ZIP/Postal Code
10559
Country
Germany
Facility Name
PowerVision Investigative Site
City
Claremont
State/Province
Cape Town
ZIP/Postal Code
7708
Country
South Africa
Facility Name
PowerVision Investigative Site
City
Northcliff
State/Province
Johannesburg
ZIP/Postal Code
2195
Country
South Africa
Facility Name
PowerVision Investigative Site
City
Queenswood
State/Province
Pretoria
ZIP/Postal Code
2001
Country
South Africa
Facility Name
PowerVision Investigative Site
City
Paardevlei
State/Province
Somerset West
ZIP/Postal Code
7130
Country
South Africa

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Clinical Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL)

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