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Application of Lightweight Multimodal Brain Function Monitoring System in Severe Stroke Patients

Application of Lightweight Multimodal Brain Function Monitoring System in Severe Stroke Patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036535
Enrollment
Unknown
Registered
2020-08-24
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

Brain Stroke

Interventions

Gold Standard:Clinical outcome
early&#32
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system

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Definitely diagnose patients with severe stroke, with GSC score <= 8; 2. With the consent of the hospital's ethics committee, the patient or his designated immediate family members will sign an informed consent form; 3. Aged 18-80 years; 4. In the department of intensive care medicine, the patient and his family agree to continue conservative treatment or surgical treatment;

Exclusion criteria

Exclusion criteria: 1. The severity of the primary disease is relatively high, and the primary disease may cause death within 48 hours if it is not out of the dangerous period; 2. People with previous severe organ dysfunction, including severe liver and kidney dysfunction, heart dysfunction, coagulation dysfunction, etc.; 3. Patients with brain tumors or patients with brain tumors; 4. Patients with previous mental disorders, Alzheimer's and other underlying diseases that affect consciousness.

Design outcomes

Primary

MeasureTime frame
EEG;StO2;TCD;SEN, SPE, ACC, AUC of ROC;

Countries

China

Contacts

Public ContactYe Gong

HuaShan Hospital, Fudan University

gong_ye@fudan.edu.cn+86 13817939896

Outcome results

None listed

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