Alzheimer's Disease Trial, Recruiting NCT07294885 Sponsor: General Hospital of Shenyang Military Region Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT07294885
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 50 and 80 years old (inclusive), of any gender
  • People who have been diagnosed with Mild Cognitive Impairment or mild to moderate dementia caused by Alzheimer's disease, based on 2024 diagnostic guidelines
  • People whose symptoms have lasted at least 6 months and have not improved after 3 or more months of standard treatment
  • People whose score on a standard memory and thinking test (called the MMSE) falls between 12 and 26
  • People who have had brain scan or spinal fluid tests confirming the presence of Alzheimer's-related proteins in the brain
  • People who have a reliable caregiver who spends at least 3 hours per day with them
  • People (or their legal representative) who have signed a written consent form agreeing to take part

Who may not be able to join:

  • People for whom MRI scans, a specific eye/vessel imaging test (ICG angiography), or PET scans are not medically safe
  • People for whom surgery or general anaesthesia is considered unsafe, such as those with blood clotting problems (confirm with trial site for specific blood test thresholds)
  • People with serious problems affecting major organs, such as significantly reduced heart function, or severe liver or kidney disease (confirm with trial site for specific test thresholds)
  • People whose MRI shows structural problems in the brain, such as tumours, strokes, bleeding, aneurysms, abnormal blood vessels, or fluid build-up
  • People whose MRI shows significant signs of small vessel disease in the brain, including certain patterns of white matter changes or four or more small bleeds in the brain
  • People whose dementia or memory problems are caused by something other than Alzheimer's disease, such as a thyroid condition or vitamin B12 deficiency
  • People with a drug or alcohol addiction
  • People with a severe psychiatric illness or who are considered at risk of suicide
  • People who have another serious medical condition that means they are not expected to live longer than one year
  • People who have taken part in another interventional clinical trial within the past 3 months
  • People who the trial investigators consider unlikely to follow the trial requirements, or who are otherwise judged unsuitable for participation
  • People currently receiving treatment with the medications Lecanemab or Donanemab
  • People with any other condition the trial investigator considers unsuitable for participation (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 6 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
General Hospital of Shenyang Military Region
Registry
ClinicalTrials.gov
Start date
20 March 2026
Est. completion
30 August 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Changes in Montreal Cognitive Assessment (MoCA) score; Changes in Mini-mental State Examination (MMSE) score; Changes in Barthel index (BI); Changes in Clinician's Interview-Based Impression of Change-plus caregiver input (CIBIC-plus)

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: 6 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