Comparison Between Foresee Home and Optical Coherence Tomography (OCT) Visual Field Defects in Patients With Choroidal Neovascularization (CNV)

NCT01073592 — Completed, 10 participants, Notal Vision Ltd.

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Comparison Between Home Macular Perimeter (FORESEE HOME) and OCT Visual Field Defects in Patients With CNV

RegistryNCT01073592
StatusCompleted
Study typeObservational
Enrollment10 (Actual)
SponsorNotal Vision Ltd. (Industry)
ConditionsAge Related Macular Degeneration
Datesstart 2009-08-01, primary completion 2013-01-01, completion 2013-03-01, first posted 2010-02-23, last updated 2013-05-17
Locations1 site in Israel

Related Papers Related Patents Related Grants Related Experts
All trials for Age Related Macular Degeneration

-Summary

The Foresee Home is used in the recent years to detect age-related macular degeneration (AMD) lesions. The device is capable of differentiation as to stages of AMD and early detection of changes including choroidal neovascularization (CNV). The Foresee Home demonstrates a high level of sensitivity and specificity as to the different stages of AMD including newly diagnosed or early detection of CNV.

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.

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+Arms and interventions

ArmTypeInterventionsDescription
CNV patiens

+Outcome measures

Primary outcomes

  • Size and location of lesions [6 months]

+Eligibility

Sex: All, ages: 50 Years to any

Inclusion Criteria:

* Capable and willing to sign a consent form and participate in the study
* Subjects diagnosed with CNV
* Did not perform more then 4 anti- VGEF injections
* VA with habitual correction better then 6/45 in the study eye
* Ability to understand instructions
* Familiar with computer usage

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
* Participation in another study with the exclusion of AREDS study

+Locations (1)

FacilityCityCountryStatus
Rabin Medical CenterPetah TikvaIsrael

+Investigators