Age Related Macular Degeneration Clinical Trial
Official title:
Pilot Study of WA-NG Telescope Prosthesis in Patients With Central Vision Impairment Associated With End-stage Age-related Macular Degeneration
NCT number | NCT01361256 |
Other study ID # | WA-NG-001 |
Secondary ID | |
Status | Withdrawn |
Phase | Early Phase 1 |
First received | |
Last updated | |
Start date | May 2011 |
Est. completion date | May 2016 |
Verified date | October 2016 |
Source | VisionCare, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a pilot study to evaluate the safety of the Model WA-NG telescope prosthesis in patients with bilateral moderate to profound central vision impairment due to end-stage age-related macular degeneration.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | May 2016 |
Est. primary completion date | April 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: - Bi-lateral, stable, moderate to profound (20/80 to 20/800) central vision impairment due to bilateral scotoma associated with end-stage macular degeneration, defined as retinal finds of bilateral, geographic atrophy or disciform scar with foveal involvement. Phakic in the operative eye. Must achieve a 5 letter improved with external telescope simulator. More medical Exclusion Criteria: - Evidence of active CNV or any ophthalmic pathology that compromises peripheral vision of fellow eye or predisposes eye rubbing. Previous intraocular of corneal surgery of any kind in operative eye. Retinal disease, optic nerve disease, diabetic retinopathy, retinal tears, or any intraocular tumor or medical or ophthalmic condition that in the opinion of the investigator renders the subject unsuitable for participation. |
Country | Name | City | State |
---|---|---|---|
Israel | Sheba Medical Center | Tel Hasomer |
Lead Sponsor | Collaborator |
---|---|
VisionCare, Inc. |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Positional Stability | Positional stability assessed by slit lamp examination and anterior segment OCT | 12 months | |
Secondary | Adverse events | adverse events | 12 months |
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