Clinical Trials Directory

Trials / Completed

CompletedNCT01010997

Foresee Home for Monitoring Age Related Macular Degeneration (AMD)

Status
Completed
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
Notal Vision Ltd. · Industry
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DEVICEForesee Homeusing the Foresee home device

Timeline

Start date
2009-12-01
Primary completion
2012-01-01
Completion
2012-01-01
First posted
2009-11-10
Last updated
2012-07-31

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01010997. Inclusion in this directory is not an endorsement.