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NCT05518409

Immunohistochemical Study of Neurodegenerative Diseases

Status unknown NA Last updated 14 September 2023
What this trial tests

NA trial testing Detection of cytof in peripheral PBMC in Alzheimer Disease in 100 participants. Status unknown.

Timeline
1 April 2022
Primary endpoint
1 December 2023
30 December 2023

Quick facts

Lead sponsorFirst Affiliated Hospital of Zhejiang University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment100
Start date1 April 2022
Primary completion1 December 2023
Estimated completion30 December 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

First Affiliated Hospital of Zhejiang University

Who can join

Adults 55 to 100, any sex, with Alzheimer Disease or Lewy Body Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The subject uses cytof to analyze PBMC of sporadic AD and DLB, which is used to reveal the differences in immune characteristics of the two diseases at the single-cell level, build immune models for specific diseases, and define these two neurodegenerative diseases with high precision from the level of molecular immunity. To provide basis for further study of the immunohistochemical differences between the two diseases, and provide objective support for clinical diagnosis and differential diagnosis.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Peripheral Single-Cell Immune Characteristics Contribute to the Diagnosis of Alzheimer's Disease and Dementia With Lewy Bodies.
    Qiu C, Zhang D, Wang M, Mei X, et al · · 2025 · cited 5× · PMID 39754303 · DOI 10.1111/cns.70204

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Other recruiting trials for Alzheimer Disease

Currently open trials in the same condition.

Other First Affiliated Hospital of Zhejiang University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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