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Perioperative application of T20A non-invasive cardiac output monitoring in patients undergoing epigastric surgery

Perioperative application of T20A non-invasive cardiac output monitoring in patients undergoing epigastric surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099022
Enrollment
Unknown
Registered
2025-03-17
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

None

Interventions

Observation group:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients with gastrointestinal surgery in the Department of general surgery, Shanghai General hospital. 2.The patients were aged 18-80 years.

Exclusion criteria

Exclusion criteria: 1. The patient has severe vascular lesions (such as arterial obstruction and vascular replacement). 2. The patient has severe cardiac valve disease (such as aortic regurgitation or regurgitation). 3. The patient has severe arrhythmia (such as atrial fibrillation). 4. Emergency surgery. 5. Patients with incomplete skin at the sensor placement site (patients who cannot use noninvasive cardiac output monitoring). 6. The patient has other diseases that may affect cardiac output (such as overweight or massive ascites > 10% body weight). 7. Patients who did not sign informed consent.

Design outcomes

Primary

MeasureTime frame
Cardiac output;

Secondary

MeasureTime frame
Stroke volume;Stroke variability;Peripheral vascular resistance;

Countries

China

Contacts

Public ContactYimin Qiu

Shanghai General Hospital

graceqiu@163.com+86 181 2128 5957

Outcome results

None listed

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