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Validation of cardiac output devices: comparison between new software version of FloTrac/Vigileoâ„¢ and transpulmonary thermodilution in septic shock patients

Validation of cardiac index measured by the fourth-generation of FloTrac/VigileoTM compared with a transpulmonary thermodilution device in septic shock patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20190821003
Enrollment
Unknown
Registered
2019-08-21
Start date
2014-01-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

septic shock

Interventions

4th generation of FloTrac/Vigileo
Diagnostic
FloTrac/Vigileo

Sponsors

Faculty of Medicine, Prince of Songkla university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 90 Years

Inclusion criteria

Inclusion criteria: Septic shock in ICU

Exclusion criteria

Exclusion criteria: Participation in a clinical study

Design outcomes

Primary

MeasureTime frame
Agreement and concordance 24 hr Vigileo and PiCCO—

Secondary

MeasureTime frame
N/A N/A N/A—

Countries

Thailand

Contacts

Public ContactBodin Khwannimit

Faculty of Medicine, Prince of Songkla university

kbordinbodin@gmail.com0815987253

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026