Macular Degeneration Trial, Recruiting (NCT02617966)

Macular Degeneration Trial, Recruiting NCT02617966 Sponsor: National Eye Institute (NEI) Condition: Macular Degeneration

Printed from Voxsanity (voxsanity.com.au) — NCT02617966 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.

Back to Macular Degeneration

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

You must be 5 years old or older
You (or your parent/legal guardian) must be willing and able to understand and sign a consent form for the study
You must be able to cooperate with the tests required during the study

If you have a retinal disease:

You must have a retinal disease that has been confirmed by standard eye tests, such as vision field testing, electrical activity testing of the eye, or eye imaging
You must have some level of measurable vision (even if very limited)

If you are a healthy volunteer:

You must have 20/20 vision or better in at least one eye, either naturally or with glasses or contact lenses

Who may not be able to join:

People who have changes in the parts of the eye in front of the retina (such as the lens or cornea) that are significant enough to block a clear view of the retina (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.

Last synced 26 July 2026

This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Brett G Jeffrey, Ph.D., National Eye Institute (NEI)

Phone: (301) 451-1621

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Voxsanity

Clinical trials and treatments, explained plainly · voxsanity.com.au

Date:

To: My Doctor

Re: Clinical trial enquiry

I am writing to enquire about the following clinical trial which may be relevant to my care:

Trial: NCT02617966

Sponsor: National Eye Institute (NEI)

Phase: Not Applicable

Status: Recruiting

Condition: Macular Degeneration

Trial contact: (301) 451-1621

More information: https://clinicaltrials.gov/study/NCT02617966

Eligibility summary (AI generated)

Written by an AI model from the ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

You must be 5 years old or older
You (or your parent/legal guardian) must be willing and able to understand and sign a consent form for the study
You must be able to cooperate with the tests required during the study

If you have a retinal disease:

You must have a retinal disease that has been confirmed by standard eye tests, such as vision field testing, electrical activity testing of the eye, or eye imaging
You must have some level of measurable vision (even if very limited)

If you are a healthy volunteer:

You must have 20/20 vision or better in at least one eye, either naturally or with glasses or contact lenses

Who may not be able to join:

People who have changes in the parts of the eye in front of the retina (such as the lens or cornea) that are significant enough to block a clear view of the retina (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Access in Australia: A treatment being studied in a clinical trial is generally not yet listed on the PBS. Where a medicine is not approved or not available through a trial, the TGA Special Access Scheme may allow a doctor to access unapproved therapeutic goods for individual patients. See voxsanity.com.au/sas-navigator/ for a plain English explainer.

This information was sourced from ClinicalTrials.gov via Voxsanity (data last synced 26 July 2026). It is not medical advice. Please verify the trial's current status directly with the trial site before acting.

Trial details

Status

Recruiting

Phase

Not Applicable

Sponsor

National Eye Institute (NEI)

Registry

ClinicalTrials.gov

Start date

24 March 2016

Est. completion

30 December 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

The primary outcomes for this study are to establish normal ranges for the kinetics of dark adaptation and dark-adapted retinal sensitivity for the fundus guided and non-guided perimeters and for RF hyperacuity on the Display++.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov