Macular Degeneration Trial, Recruiting NCT06351657 Sponsor: Medical University of Vienna Condition: Macular Degeneration
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Macular Degeneration Trial, Recruiting

NCT06351657
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 aged between 55 and 99 years old.
  • People who have a specific type of eye condition called complete RPE and outer retinal atrophy (cRORA) — this is a particular pattern of damage to a layer at the back of the eye, confirmed through detailed eye imaging (confirm with trial site for exact measurements required).
  • If both eyes meet the criteria, both eyes may be included in the study.
  • People whose eyes are clear enough (no clouding of the lens or other obstructions) and whose pupils can be dilated sufficiently for imaging and vision testing.

Who may not be able to join:

  • People who have had eye surgery in the study eye within the 3 months before the study starts.
  • People who have previously received anti-VEGF injections (a type of eye injection treatment) in the study eye.
  • People who have a history of a specific type of swelling in the eye after cataract surgery (known as pseudophakic cystoid macular edema or Irvine Gass Syndrome) in the study eye.
  • People who have uncontrolled glaucoma in the study eye, meaning eye pressure has remained high (25 mmHg or above) even with pressure-lowering medication, or where a certain measurement of the optic nerve exceeds a specific threshold (confirm with trial site).
  • People who have another eye condition in the study eye that the study doctor believes is likely to need medical or surgical treatment during the study to prevent vision loss.
  • People who have another eye condition in the study eye that the study doctor believes could interfere with the study results or require surgery (other than cataract surgery or a specific laser procedure called YAG capsulotomy).
  • People who have corneal damage, cloudiness, or scarring in the study eye that affects their best corrected vision.
  • People with a refractive error (the degree of short- or long-sightedness) greater than 6 diopters — this also applies to people who have had cataract surgery or refractive surgery if their prescription history exceeded 6 diopters.
  • People currently taking medications known to damage the retina, such as hydroxychloroquine or tamoxifen.
  • People who have active abnormal blood vessel growth at the back of the eye (macular neovascularization) at the time of study entry.

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: +43 1 40400-73419

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

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
11 April 2025
Est. completion
1 July 2027

Where this trial is recruiting

🇦🇹 Austria 🇫🇷 France 🇸🇮 Slovenia 🇪🇸 Spain 🇨🇭 Switzerland 🇬🇧 United Kingdom

Primary endpoints

To characterise and quantify focal and global changes of the retina by retinal imaging to identify patients at risk for fast geographic atrophy (GA) progression

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