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NCT05690880Active, not recruiting

ForeseeHome NRich Registry

Source: ClinicalTrials.gov · Last updated 15 Feb 2023

Brief summary (registry, in English)

This registry will compare functional and structural data of progression of Intermediate AMD (iAMD) and conversion to neovascular AMD (NV-AMD) while monitored at home with the ForeseeHome Monitoring System (FSH) and during routine care with Spectral Domain Optical Coherence Tomography (SD-OCT) and to validate the predictive value of a non-NV-AMD FSH alerts.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
20000 (estimated)
First submitted
10 Jan 2023
Start date
15 Dec 2022
Primary completion date
15 Dec 2027
Lead sponsor
Notal Vision Inc.
NCT number
NCT05690880

What you commit to

  • Study type: Observational
  • Planned participants: 20000
  • From 15 Dec 2022 to the primary completion date, 15 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients that are unable to establish a baseline

Who the study is looking for

  • The participants include those actively monitoring on the FSH program which requires diagnosis of intermediate AMD and visual acuity of 20/60 or better that establish a valid baseline in at least one eye.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
NJ Retina
Coordinator of this site? Confirm its status
Toms RiverUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.