Macular Degeneration Trial, Recruiting NCT04697095 Sponsor: Hospices Civils de Lyon Condition: Macular Degeneration
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Macular Degeneration Trial, Recruiting

NCT04697095
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:

  • You are male or female and older than 50 years of age
  • You are willing and able to sign a written consent form to participate
  • You are registered with the French social security system
  • Your blood sample amounts (for both care and research) can be managed safely based on your body weight
  • You have the same type of age-related macular degeneration (AMD — a condition affecting the back of the eye) in both eyes, OR early AMD in one eye and a more advanced form in the other, OR you have no eye disease at all (for the control group)

Who may not be able to join:

  • You weigh less than 50 kg (approximately 110 lbs)
  • You are an adult under legal guardianship or are unable to give consent for yourself
  • You are currently detained or deprived of your liberty
  • You are already taking part in another clinical trial at the time of joining this study
  • You have one type of advanced AMD (dry/atrophic) in one eye and a different type (wet/exudative) in the other eye
  • You have other long-term retinal (back of the eye) conditions beyond AMD
  • You are taking medicines that affect your immune system, such as immunosuppressants, chemotherapy, or long-term steroids
  • You have a health condition that affects how your immune system works
  • You have a history of diabetes
  • You have had a specific light-based eye treatment called photodynamic therapy on the eye being studied

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 12 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: Thibaud Mathis, MD, Service d'Ophtalmologie Hospices Civils de Lyon Hôpital de la Croix Rousse

Phone: 4 26 10 93 22

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
Registry
ClinicalTrials.gov
Start date
1 June 2022
Est. completion
2 December 2025

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Comparison of the survival of human monocytes on ARPE-19 cultures, between the group of patients with atrophic AMD and patient with no retinal pathology (control).

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: 12 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