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Intraoperative monitoring of continuous transesophageal oxygen delivery: an observational study

Intraoperative monitoring of continuous transesophageal oxygen delivery: an observational study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084884
Enrollment
Unknown
Registered
2024-05-27
Start date
2024-05-28
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

noncardiac surgery

Interventions

Observation group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) American Society of Anesthesiology (ASA) physical status of ?~ ?; (2) Aged between 18-70 years old, men or women; (3) patients scheduled for elective non-cardiac surgery under general anesthesia, and invasive monitoring of arterial blood pressure, blood gas or cardiac output is required during the procedure due to medical necessity.

Exclusion criteria

Exclusion criteria: (1) Upper digestive system diseases and operations, including esophageal diseases, gastric ulcers, gastrofundus and esophageal varices, etc. (2) Severe coagulation disorders. (3) Conditions that are not suitable for Picco monitoring: arrhythmia, severe valvular regurgitation, etc.

Design outcomes

Primary

MeasureTime frame
Oxygen delivery (DO2);cardiac output (CO);hemoglobin (Hb);heart rate (HR);arterial oxygen saturation (SaO2);SV;

Secondary

MeasureTime frame
the incidence of complications related to probe placement, including throat pain and esophageal mucosa injury;IBP, BP (systolic blood pressure, diastolic blood pressure, mean arterial pressure), lactate;Hospitalization time and extubation time;Major cardiovascular adverse events;

Countries

China

Contacts

Public ContactPeng Ling

West China Hospital of Sichuan University

penglingjq@163.com+86 150 0286 9535

Outcome results

None listed

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