Alzheimer's Disease Trial, Recruiting NCT06661564 Sponsor: University Hospital, Tours Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT06661564
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 18 years of age or older
  • People who are enrolled in the French Social Security scheme
  • People who have given their informed consent to participate, confirmed in writing

Who may not be able to join:

  • People who are pregnant or breastfeeding
  • People who are under judicial protection measures
  • People who are under guardianship or curatorship
  • People who have another neurodegenerative disease (a condition affecting the brain or nervous system other than the one being studied)
  • People who use eye drops or any treatment that could affect tear production
  • People who have worn contact lenses occasionally or regularly in the last 3 months
  • People who have had eye surgery within the last 3 months
  • People who have an eye condition other than refractive errors (such as needing glasses), eye movement disorders, or amblyopia (lazy eye)
  • People who have a general health condition, other than the condition being studied, that affects the eyes
  • People who are unable to have their tears collected for the study

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 13 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: Victoire LEROY, MD, CHRU de Tours

Phone: 0247477693

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
University Hospital, Tours
Registry
ClinicalTrials.gov
Start date
9 July 2025
Est. completion
1 July 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Concentration of total Tau proteins in basal tears of patients with AD vs healthy volunteers; Concentration of phosphorylated Tau proteins in basal tears of patients with AD vs healthy volunteers; Concentration of Amyloid β 1-40 proteins in basal tears of patients with AD vs healthy volunteers; Concentration of Amyloid β 1-42 in basal tears of patients with AD vs healthy volunteers; Lipids in basal tears of patients with AD vs healthy volunteers; Metabolites in basal tears of patients with AD vs healthy volunteers

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: 13 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