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Early diagnosis and clinical observation of cognitive dysfunction after stroke

Early diagnosis and clinical observation of cognitive dysfunction after stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-17012227
Enrollment
Unknown
Registered
2017-08-02
Start date
2017-08-10
Completion date
Unknown
Last updated
2017-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ischemic stroke

Interventions

Acute ischemic stroke group:data collection and follow-up

Sponsors

Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) first onset, within 72 hours in patients with acute ischemic stroke; 2) Aged 45-80 years old; 3) sign informed consent.

Exclusion criteria

Exclusion criteria: 1) dementia or severe cognitive impairment occurs prior to stroke; 2) hemorrhagic stroke; 3) consciousness disorder; 4) aphasia or dysarthria; 5) end-stage severe disease; 6) severe depressive disorder; 7) failed to finish high resolution nuclear magnetic examination.

Design outcomes

Primary

MeasureTime frame
Neurologic impairment assessment;Neuropsychological assessment;Functional MRI;—

Countries

China

Contacts

Public ContactYUN XU

Affiliated Drum Tower Hospital of Nanjing University Medical School

xuyun20042001@aliyun.com+86 025 83105208

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026