Macular Degeneration Trial, Recruiting NCT07680244 Sponsor: Carl Zeiss Meditec-Dublin CoCe Condition: Macular Degeneration
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Macular Degeneration Trial, Recruiting

NCT07680244
Recruiting Not Applicable

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:

  • People who are able and willing to attend all required study visits
  • People who are able and willing to sign a consent form and follow the study instructions
  • People who are able and willing to have eye imaging performed
  • Adults aged 18 years or older
  • People who have no abnormalities in the central area of the retina (the macula) — Group A
  • People who have certain changes or abnormalities in the central area of the retina (the macula), such as changes at the boundary between the eye's gel and retina, fluid pockets within or beneath the retina, damage to specific retinal layers, or changes to the retinal pigment layer — Group B

Who may not be able to join:

  • People who are unable to complete the required tests
  • People who are unable to give consent or follow the study instructions
  • People who have difficulty keeping their eye still enough to allow acceptable retinal scans to be taken
  • People who have received a Visudyne (verteporfin) injection in the study eye within the last 48 hours
  • People who have used Pilocarpine or Vuity eye drops in the study eye within the last 24 hours
  • People who have significant cloudiness in the eye that prevents a clear view of the retina
  • People who have vitreous floaters (small shapes drifting in the field of vision) that prevent acceptable scans from being taken

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 28 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

Phone: 925-307-1588

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.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Carl Zeiss Meditec-Dublin CoCe
Registry
ClinicalTrials.gov
Start date
23 May 2025
Est. completion
1 August 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Sensitivity of PathFinder 1.0; Specificity of PathFinder 1.0

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: 28 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