Foresee Home for Monitoring Age Related Macular Degeneration (AMD)

Notal Vision

Status: Completed

Conditions: Age Related Macular Degeneration

Treatments: Device: Foresee Home

Study type: Observational

Funder types: Industry

Identifiers

NCT01010997

FORESEE HOME- 02

75909 (Other Identifier)

Details and patient eligibility

About

The FORESEE HOME is intended for the early detection of central and paracentral irregularities (abnormalities) in the visual field, most commonly associated with AMD. However, the device has ability to detect the development of the lesion post treatment and therefore to asses in determination of the next treatment.

Full description

The FORESEE HOME is intended for the early detection of central and paracentral irregularities (abnormalities) in the visual field, most commonly associated with AMD. However, the device has ability to detect the development of the lesion post treatment and therefore to asses in determination of the next treatment.

The OCT May be use as well to identify choroidal neovascularization (CNV). Comparison between the two methods will allow better understanding of both devices.

The FORESEE HOME can use as an assessment tool for the progression and success of the treatment given to AMD lesions. Therefore, evaluation the size and the location of the treated lesions may serve as an additional tool.

Enrollment: 10 patients

Sex: All

Ages: 50+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Capable and willing to sign a consent form and participate in the study
• Subjects diagnosed as CNV under treatment or Intermediate AMD in at least one eye
• Did not perform more then 10 anti- VEGF injections
• Age >50 years
• VA with habitual correction >6/45 in the study eye
• Computer users

Exclusion criteria

• Evidence of macular disease other than AMD or glaucoma in the study eye
• Presence of any significant media opacity that precludes a clear view of the macular area as identified in the study eye by biomicroscopy,
• Any non-macular related ocular surgery performed within 3 months prior to study entry in the target eye

Trial design

10 participants in 2 patient groups

Dry AMD

Description:

Intermediate AMD subjects

Treatment:

Device: Foresee Home

Wet - treated AMD

Description:

AMD subjects under treatments

Treatment:

Device: Foresee Home