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Clinical Trials/NCT01941472
NCT01941472
Completed
N/A

Transcutaneous pO2, Transcutaneous pCO2 and Central Venous SO2 Variations to Define Fluid Responsiveness

Peking Union Medical College Hospital1 site in 1 country40 target enrollmentSeptember 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hypotension
Sponsor
Peking Union Medical College Hospital
Enrollment
40
Locations
1
Primary Endpoint
Fluid Responsiveness
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Fluid challenge is often carried out in critical ill patients. Its responsiveness usually requires invasive monitoring. To use non-invasive methods is very tempting. Investigators hypothesize that transcutaneous pO2,transcutaneous pCO2 and Central Venous SO2 variations provide feasible estimation on fluid responsiveness in critical ill patients.

Registry
clinicaltrials.gov
Start Date
September 2013
End Date
December 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bin Du

Director of Medical ICU

Peking Union Medical College Hospital

Eligibility Criteria

Inclusion Criteria

  • 18 years and older ICU patients;
  • Septic shock;
  • Monitored with PICCO or Swan-Ganz catheter;
  • The decision of fluid challenge made by the treating physician;

Exclusion Criteria

  • Evidence of fluid overload;
  • Pregnancy

Outcomes

Primary Outcomes

Fluid Responsiveness

Time Frame: Immediately after fluid challenge, average 5 minutes

Increase in cardiac index ≥ 10% after fluid challenge

Study Sites (1)

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