A Study of the SING IMT in an Israeli Cohort

VisionCare

Status

Not yet enrolling

Conditions

Age-Related Macular Degeneration

Geographic Atrophy

Treatments

Device: smaller incision, new generation implantable miniature telescope (SING-IMT)

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT05941273

CDV-SNG 001

Details and patient eligibility

About

The objective of this single center study is to determine the safety of the smaller incision, new generation (SING), implantable miniature telescope (IMT) in a small sample of patients with moderate-severe central vision loss due to late-stage age-related macular degeneration (AMD) in an Israeli Cohort

Full description

The SING IMT has CE Mark in the EU and has been implanted in over 200 patients globally including a pivotal study in the U.S. currently underway (the Concerto Study) and a post-marketing study in EU (The PMCF Study). Model SING is a new injectable model based on the IMT parent model (PMA P050034). Following completion of informed consent, patients will be evaluated for eligibility to enroll into the study, including assessment of their best-corrected distance- and near- visual acuity with refraction, and also when using an external telescope simulator to determine if they are likely to benefit from receiving the SING IMT. If eligible, they will be scheduled for out-patient surgery to implant the IMT during routine cataract surgery in one eye. Following implantation, patients will return for 5 post-operative follow-up visits over a period of approximately 12 months. Additionally, patients will have up to 10 rehabilitation/training visits with a low vision specialist to learn how to use the fellow eye for ambulation and the eye with the implant for magnified viewing during daily activities.

Enrollment

5 estimated patients

Sex

All

Ages

55+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For Both Eyes:

Be at least 55 years of age at the Pre-operative Visit;
Have ETDRS BCDVA 0.6 to 1.6 logMAR (20/80 to 20/800) at the Pre-operative Visit;
Have bilateral retinal findings of geographic atrophy or disciform scar with foveal involvement, as determined by fluorescein angiography (FA) or OCT;
Have an Endothelial Cell Density (ECD) above 1800 cells per millimeter;
Have central anterior chamber depth (ACD) >2.5 mm from the posterior surface of the cornea (endothelium) to the anterior surface of the crystalline lens at the Pre-operative Visit;
Agree to participate in post-operative visual training

For the Implanted Eye:

Have evidence of visually significant cataract at the Pre-operative Visit;
Agree to undergo pre-operative assessment with low vision specialists (optometrist, occupational therapist or other professional with low vision experience) in the use of an external telescope model sufficient for patient assessment and patient must achieve at least a 5-letter ETDRS BCDVA improvement (0.1 logMAR) in the final assessment

For the Non-Implanted Eye:

-Have adequate peripheral vision at the Pre-operative Visit to allow navigation.

Exclusion criteria

For Both Eyes:

Have cognitive impairment that would interfere with the ability to understand and provide Informed Consent or prevent proper visual training/rehabilitation with the device;
Have evidence of bilateral active choroidal neovascularization (CNV) on fluorescein angiography or OCT or were treated for CNV within the past six months.
Have any of the following conditions at the Pre-operative Visit:
1. Stargardt macular dystrophy;
2. Diabetic retinopathy;
3. Untreated retinal tears;
4. Retinal vascular disease;
5. Optic nerve disease;
6. History of retinal detachment;
7. Intraocular tumor;
8. Retinitis pigmentosa;
9. History of steroid-induced rise in intraocular pressure (IOP), uncontrolled glaucoma, or IOP >22 mmHg at the Pre-operative Visit;
Have known allergy to post-operative medications;
History of eye rubbing or an ocular condition that predisposes subject to eye rubbing;
Have had prior or expected ophthalmic surgery within 30 days of the Operative Visit;
Have any circumstance that, based on the Investigator's judgment, poses a concern for the subject's safety;
Any systemic disease or clinical evidence of any condition at the Pre-operative Visit which would make the subject in the opinion of the investigator unsuitable for the study;
Concurrent participation or prior participation in any investigative drug or device study within last 30 days prior to Pre-operative Visit.

For the Implanted Eye:

Have a history of corneal stromal or endothelial dystrophies, including guttata;
Have Myopia > 6.0 D or Hyperopia > 4.0 D by Manifest Refraction at the Pre-operative Visit;
Have an Axial Length (AL) < 21 mm at the Pre-operative Visit;
Have a narrow angle defined as < grade 2 on the Schaffer scale at the Pre-operative Visit;
Ongoing Inflammatory ocular disease at the Pre-operative Visit;
Zonular weakness/instability of crystalline lens, or pseudoexfoliation at the Pre-operative Visit;
Have any condition at the Pre-operative Visit which in the judgement of the Investigator indicates that the haptics cannot be placed within the capsular bag during surgery;
Have had previous intraocular or corneal surgery, including any type of surgery for refractive or therapeutic purposes;

For the Non-Implanted Eye:

-Have ophthalmic pathology at the Pre-operative Visit that compromises the patient's peripheral vision based on the Investigator's judgment.