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Effect of distal ischemia preadaptation on cognitive dysfunction after new-onset stroke

Effect of distal ischemia preadaptation on cognitive dysfunction after new-onset stroke

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099600
Enrollment
Unknown
Registered
2025-03-26
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Acute ischemic stroke

Interventions

Experimental group: Part I (Acute Phase Intervention) Part II (Post-discharge Intervention) Control group:Test group: Part 1 (Acute Phase Intervention) Conventional medical treatment, including anti
Control group:Conventional medical treatment alone with donepezil hydrochloride to control cognitive progression.

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Subjects must meet all of the following criteria: General Inclusion Criteria: 1) Age 18-80 years old (including cut-off value) 2) Diagnosed with ischemic stroke (meeting the diagnostic criteria of the 2023 Chinese Guidelines for the Diagnosis and Treatment of Ischemic Stroke), and the onset time was within 48 hours. NIHSS score 3-25 (including cut-off value) 4) Subjects or family members sign the informed consent form

Exclusion criteria

Exclusion criteria: General Exclusion Criteria: 1) Hemorrhagic stroke; 2) Stroke onset with epilepsy and inaccurate NIHSS score for which an accurate NIHSS score cannot be obtained; 3) accompanied by coma or mental disorder, which may interfere with neurological assessment; 4) Patients with central nervous system diseases; 5) Those with cognitive dysfunction caused by other reasons; 6) Those who are intolerant to the treatment regimen involved in this study; 7) Pregnant or lactating people; 8) Poor compliance; 9) Severe hepatic and renal insufficiency, including but not limited to: liver cirrhosis, hepatic encephalopathy, ascites, renal failure or uremia (Ccr<25ml/min), hepatorenal syndrome, etc.; 10) Is participating in an interventional clinical trial and has used an investigational drug or medical device; 11) Subjects may not be able to complete this study for other reasons or those who should not be included in the opinion of the investigator;

Design outcomes

Primary

MeasureTime frame
Magnetically sensitive-weighted imaging SWI;MoCA score;MoCA score;

Countries

China

Contacts

Public ContactCheng Yanbo

The Affiliated Hospital of Xuzhou Medical University, Xuzhou City, Jiangsu Province

46140705@qq.com+86 150 5082 5328

Outcome results

None listed

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