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Protein and microRNA Markers for Early Detection of Alzheimer's Disease

Sun Yat-sen University logo

Sun Yat-sen University

Status

Withdrawn

Conditions

Mild Cognitive Impairment

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT03388242
SYSEC-KY-060

Details and patient eligibility

About

Blood will be harvested from three groups of people, normal control, patients with mild cognitive impairment (MCI) and patients with Alzheimer's disease (AD), 20 people per group. The blood samples will be used to determine the difference in the expression of microRNAs and proteins. Blood samples will be harvested again at 6-month interval from patients. The combination of the microRNAs and proteins that have different expression patterns between normal control and patients with MCI will be constructed in a kit to detect the difference. This kit will be used in another set of the three groups of people to determine its sensitivity and specificity in detecting patients with MCI.

Full description

As discussed above, patients' blood samples will be tested by chip to test microRNA expression and liquid chromatography-mass spectrometry to determine protein expression. The differences in microRNA and protein expression among the three groups, especially between the control and MCI, will be analyzed. This information will be used to construct a kit that can contain probes to detect a few microRNAs or proteins. This kit will be used in another set of patients to check its sensitivity and specificity. The first set of patients will also be followed up every 6 months for up to 1.5 years. Blood samples will be harvested during the follow-ups. The changes in microRNAs and proteins will be correlated with the changes of cognition. This information will be used for constructing the kit as well.

Sex

All

Ages

30 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age-matched with patients with MCI group

Exclusion criteria

  • With cognitive dysfunction
  • With major cardiovascular diseases, especially stroke and brain transient ischemic attack
  • On steroid treatment
  • with major organ diseases

Trial design

0 participants in 3 patient groups

Normal control people
Description:
These people are age-matched with the patients with MCI. No intervention is applied.
Treatment:
Other: No intervention
Patients with MCI
Description:
These patients have met the criteria for diagnosing MCI. No intervention is applied.
Treatment:
Other: No intervention
Patients with AD
Description:
These patients are diagnosed with AD. No intervention is applied.
Treatment:
Other: No intervention

Trial contacts and locations

2

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Central trial contact

Mingyan Guo

Data sourced from clinicaltrials.gov

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