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bedside continuous cardiovascular ultrasound monitoring

bedside continuous cardiovascular ultrasound monitoring

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095166
Enrollment
Unknown
Registered
2025-01-02
Start date
2025-01-15
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Cardiovascular diseases

Interventions

TEE Monitoring Group and Wearable Monitoring Group (the same patient):None

Sponsors

Department of Anesthesiology, West China Hospital, Sichuan University.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. All age groups; 2. Plan to recruit 100 non-cardiac surgery patients; 3. Intraoperative TEE monitoring.

Exclusion criteria

Exclusion criteria: 1. Patients with chest skin conditions unsuitable for attaching wearable devices (such as severe skin diseases, open wounds, etc.); 2. Known allergy to ultrasound gel; 3. Poor ultrasound image quality, making accurate identification and measurement impossible; 4. Patient's refusal to participate.

Design outcomes

Primary

MeasureTime frame
Fractional Area Change;

Secondary

MeasureTime frame
Ultrasound Image Quality and Structural Clarity;

Countries

China

Contacts

Public ContactHaibo Song

Department of Anesthesiology, West China Hospital, Sichuan University.

pdasonghaibo@163.com+86 189 8060 1682

Outcome results

None listed

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