FindTrial
Sign In

Comparison of stroke volume measurements by TEE and FloTrac/ Vigileo before and after abdominal aortic balloon occlusion

Comparison of stroke volume measurements by TEE and FloTrac/ Vigileo before and after abdominal aortic balloon occlusion

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-DDD-17011353
Enrollment
Unknown
Registered
2017-05-11
Start date
2017-06-01
Completion date
Unknown
Last updated
2017-05-22

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

Conditions

acral or pelvis tumor

Interventions

Gold Standard:Transesophageal Echocardiography, TEE
Index test:FloTrac

Sponsors

Dept of Anesthesiology, Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ASA I or II, aged 18-60, ungergoing selective acral or pelvis tumor resection under general anesthesia.

Exclusion criteria

Exclusion criteria: Arrhythmia, heart disease, stenosis or occlusion of esophagus, Esophageal varices or hemorrage,hemorrahge,history of esophageal or gastrointestinal surgery

Design outcomes

Primary

MeasureTime frame
comparability of FloTrac/Vigileo and transesophageal echocardiography measurements of stroke volume;—

Countries

China

Contacts

Public ContactJiang Luyang

Dept of Anesthesiology, Peking University People's Hospital

jly1018@sina.com+86 13269054309

Outcome results

None listed

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