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The clinical application of quantitative electroencephalography (qEEG) in early neurological monitoring and prediction of prognosis in acute ischemic stroke (AIS)

The clinical application of quantitative electroencephalography in acute ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070829
Enrollment
Unknown
Registered
2023-04-24
Start date
2023-05-01
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

acute ischemic stroke

Interventions

Electroencephalographic examination:Collection of qEEG signals

Sponsors

Tianjin Huanhu Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: General inclusion criteria. A. Patients aged greater than or equal to 18 and less than or equal to 85 years. B. Proven acute ischemic stroke within 24 hours of onset. C. New focal neurological deficits consistent with acute cerebral ischemia. D. modified Rankin score of 0-2 before onset. E. Informed consent obtained from the patient or the patient's legally authorized representative. F. All subjects or their proxies are required to sign an informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria. A. Acute cerebral hemorrhage or subarachnoid hemorrhage, active hemorrhage or pre-existing bleeding tendency. B. non-first episode with a history of old cerebral hemorrhage/ischemia. C. Non-vascular disease causing, e.g., tumor, trauma, hematologic disease. D. Pre-existing immune disorders that confound outcome evaluation, neurological or psychiatric disorders, stroke attacks with epilepsy or other psychiatric disorders and irritable states unable to cooperate with the examination E. Coma or altered level of consciousness or unstable vital signs. F. Hepatic or renal insufficiency, active infection, severe cardiac arrhythmias. G. Women who are known to be pregnant, breastfeeding or have an active or indeterminate pregnancy test.

Design outcomes

Primary

MeasureTime frame
mRS score;

Secondary

MeasureTime frame
qEEG examination;MRI;NCCT;NIHSS score;

Countries

China

Contacts

Public ContactYing Huang

Tianjin Huanhu Hospital

yinghuang0000@163.com+86 13803041267

Outcome results

None listed

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