Alzheimer's Disease Trial, Recruiting NCT07643363 Sponsor: Tianjin Huanhu Hospital Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT07643363
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 have been diagnosed with probable Alzheimer's disease (AD) with mild cognitive impairment, based on 2024 guidelines, OR you have been diagnosed with a type of frontotemporal dementia (a condition affecting behaviour or language).
  • Test results (from a brain scan or spinal fluid test) show abnormal amyloid protein buildup in the brain — this is a marker linked to Alzheimer's disease (confirm with trial site).
  • Test results (from a brain scan or spinal fluid test) show abnormal tau protein in the brain — another marker linked to Alzheimer's disease (confirm with trial site).
  • If you have Alzheimer's disease, you have been taking standard Alzheimer's medications at the same dose for at least 12 weeks before the study starts.
  • If available, genetic test results confirming a frontotemporal dementia-related gene mutation may be included (this appears to be optional — confirm with trial site).
  • You are between 45 and 85 years old; there is no restriction on gender.
  • You are right-handed.
  • You have had at least 3 years of formal education.
  • You scored 11 or higher on a standard memory and thinking test called the MMSE (confirm with trial site).
  • You have a CDR score of 1 or 2, meaning your dementia is in the mild to moderate range (confirm with trial site).
  • You have a reliable caregiver who can support your participation.
  • You are able to take part in thinking and memory tests and training activities.
  • You fully understand the study, are willing to take part voluntarily, and can sign a consent form approved by an ethics committee.

Who may not be able to join:

  • You have been diagnosed with another type of dementia or a major brain or nervous system condition, such as stroke, epilepsy, Lewy body dementia, vascular dementia, Parkinson's disease dementia, or Huntington's disease.
  • You have a significant mental health condition, such as severe depression or severe anxiety.
  • You have serious problems with your heart, liver, or kidneys (for example, advanced heart failure, liver cirrhosis, or kidney failure).
  • You take medications that are known to significantly affect memory or thinking (such as certain sedatives or specific bladder medications), unless your doctor has approved them.
  • You have metal implants in your body that are not safe for MRI scans or a specific type of brain stimulation used in this trial, such as a pacemaker or deep brain stimulator.
  • You have defects or abnormalities in your skull.
  • You are unable to tolerate wearing an EEG cap (brain activity recording device) or keeping your head still during procedures.
  • You have severe vision or hearing problems that would prevent you from completing the study tasks.
  • You have a history of alcohol or drug misuse.
  • You have taken part in another clinical trial within the past 3 months.
  • You are currently receiving or have recently received treatment with certain newer Alzheimer's drugs called anti-amyloid antibodies (for example, lecanemab or donanemab).

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 27 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: +86 18959257015

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
Tianjin Huanhu Hospital
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
1 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Changes from Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog) Score

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: 27 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