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Effect of edaravone on post-stroke cognitive impairment and plasma A-Beta levels

Effect of edaravone on post-stroke cognitive impairment and plasma A-Beta levels

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024883
Enrollment
Unknown
Registered
2019-08-01
Start date
2017-01-01
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Post-stroke cognitive impairment

Interventions

Experimental group:Conventional treatment plus edaravone
Control group:Conventional treatment

Sponsors

First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 84 Years

Inclusion criteria

Inclusion criteria: 1. A diagnosis of ischemic stroke was made according to clinical criteria; 2. MRI or CT supports the diagnosis of acute cerebral infarction; 3. Aged >=45 years old male and female; 4. IQCODE=3, can complete neuropsychological testing; 6. Stroke within 2 weeks of onset; 7. The subjects are of primary school education or above and have the ability to complete the cognitive ability determination and other tests specified in the program; 8. Patient agreed and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Imaging evaluation without new cerebral infarction and asymptomatic lacunars infarction; 2. individuals who suffered from an uncorrectable visual or hearing dysfunction, or had difficulty completing the neuropsychological test; 3. Have been diagnosed with cognitive impairment and were using cholinesterase inhibitors or memantine; 4. individuals who suffered from psychosis, e.g., schizophrenia, bipolar affective disorder, severe depression, delirium; 5. Suffering from malignant tumors and heart, liver, kidney and other organ dysfunction or severe systemic diseases; 6. Missing laboratory indicators individuals: A-beta sLRP-1sRAGEFBGTGTCHDLLDLHcy; 7. Plasma A-beta, sLRP-1, sRAGE values were extreme values (The average value exceeds 3+/-SDs).

Design outcomes

Primary

MeasureTime frame
Aß42;Aß40;sLRP-1;sRAGE;

Countries

China

Contacts

Public ContactQu Qiumin

First Affiliated Hospital of Xi'an Jiaotong University

whspring@126.com029-85324083

Outcome results

None listed

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