Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects

Status unconfirmed · Not applicable

Conditions studied: Full Aniridia, Partial Aniridia

In brief

The purpose of this study is to study the long term safety and effectiveness of an artificial iris prosthesis for the treatment of iris defects.

Key facts

Study ID: NCT01860612
Run by: Clinical Research Consultants, Inc.
People needed: 500
Starts: 2013-10-01
Expected to finish: 2025-12-31
Last updated by the study team: 2022-10-24

Who can join

Age: 3 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

For the IDE study, subjects in whom the subject and study eye meet all of the following criteria were candidates for the PMA cohort of this study, or the Continued Access cohort after the PMA cohort was enrolled:
22 years of age or older
Having a diagnosis of congenital or acquired full or partial iris defect in the study eye.
Having symptoms of light sensitivity, photophobia, and/or glare in the study eye.
Subjects should be pseudophakic, aphakic or require cataract extraction.
Signed and received a copy of the signed written informed consent.
Willingness and ability to comply with schedule for follow-up visits and postoperative evaluations.
All adult and pediatric subjects who participated in the 12-month AI-001 IDE clinical trial who meet the following inclusion criteria are eligible for enrollment in the PAS; hereafter referred to as the "Long Term Extension Cohort":
Previous AI-001 IDE study participant who was enrolled before PMA approval (i.e., before May 30, 2018) and has had the CustomFlex™ Artificial Iris implanted for 36 months or less if enrolled as an adult or for 60 months or less if enrolled as a pediatric subject.
Signed and received a copy of the signed written informed consent.
Willingness and ability to comply with schedule for follow-up visits and postoperative evaluations.
Pediatric subjects in whom the subject and study eye meet all of the following criteria are candidates for enrollment in the Pediatric New Enrollment Cohort:
Age between 3 years and less than 22 years at the time of consent for the OSB PAS.
Having a diagnosis of congenital or acquired full or partial iris defect in the study eye.
Having symptoms of light sensitivity, photophobia, and/or glare or other aniridic symptoms in the study eye.
Subjects should be pseudophakic, aphakic or require cataract extraction.
Signed and received a copy of the signed written informed consent for the OSB PAS.
Willingness and ability to comply with schedule for follow-up visits and postoperative evaluations.

You may not qualify if…

There are no exclusion criteria for the Long Term Extension Cohort .
For the IDE study, all subjects in whom the subject or study eye meets any of the following criteria will were excluded from the PMA cohort of this study, or the Continued Access cohort after the PMA cohort was enrolled:
Uncontrolled ocular inflammation (e.g., uveitis).
Preoperative intraocular pressure > 21 mm Hg.
Subjects with a current condition that, in the investigator's opinion, would interfere with the treatment.
Subjects with any of the following conditions:
Severe chronic uveitis
Microphthalmus
Untreated retinal detachment
Untreated chronic glaucoma
Rubella cataract
Rubeosis of the iris
Proliferative diabetic retinopathy
Female subjects who are pregnant or lactating at the time of surgery.
Subjects with a known sensitivity to required postoperative study medications (4th generation fluoroquinolone or steroid anti-inflammatory) if an alternative medication is not available.
Subjects under legal guardianship or who, in the investigator's opinion, lack the mental capacity to provide written informed consent for study participation.
Stargardt's retinopathy.
Subjects with gastric ulcers or diabetes mellitus in whom high doses of postoperative systemic steroids are required.
Surgical difficulty of the planned surgery, which might increase the potential for complications.
No useful vision or vision potential in the fellow eye.
Clear crystalline lens (in eyes with intact natural, crystalline lens).
Implantation of a CustomFlex™ Artificial Iris prosthesis in the contralateral eye within the previous 4 weeks.
In the investigator's opinion, the presence of a condition or finding in the contralateral eye that would make it unsafe to implant a CustomFlex™ Artificial Iris prosthesis in the study eye.
All pediatric subjects in whom the subject or study eye meets any of the following criteria will be excluded from enrollment in the Pediatric New Enrollment Cohort:
Uncontrolled ocular inflammation (e.g., uveitis).

Where it is running

Wills Eye Institute — Philadelphia, Pennsylvania, United States (enrolling)
Cincinnati Eye Institute — Cincinnati, Ohio, United States (enrolling)
Advanced Vision Care — Los Angeles, California, United States (enrolling)
Eye Consultants of Atlanta — Atlanta, Georgia, United States
Price Vision Group — Indianapolis, Indiana, United States
Minnesota Eye Consultants — Bloomington, Minnesota, United States
The Mackool Eye Institute — Astoria, New York, United States
Rosenthal Eye Surgery — Great Neck, New York, United States
Oregon Eye Associates — Eugene, Oregon, United States
Alkek Eye Center/ Baylor College of Medicine — Houston, Texas, United States
The Eye Institute of Utah — Salt Lake City, Utah, United States
Jules Stein Eye Institute — Los Angeles, California, United States
Woolfson Eye Institute — Atlanta, Georgia, United States

Full record on ClinicalTrials.gov

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