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Assessment of Transcutaneous Oxygen Tension/Oxygen Challenge Test in Intensive Care Unit (ICU) Patients (ICUPtO2OCT)

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Unknown

Conditions

Shock
Sepsis

Study type

Observational

Funder types

Other

Identifiers

NCT01174966
PUMCH-ICU-LDW-OCT

Details and patient eligibility

About

The lack of subcutaneous partial pressure of oxygen (PO2) rise in response to high fraction of inspired oxygen (FiO2), called the "oxygen challenge test (OCT)", was associated with higher morbidity and mortality in human subjects. Patients had negative O2 challenge test results, indicating that flow-dependent O2 consumption might have been present. Recent reports using the noninvasive transcutaneous PO2 (PtO2) and transcutaneous partial pressure of carbon dioxide probes have observed a relationship between low oxygen challenge test values to mortality and organ failure. The OCT values provides an accessible noninvasive method of detecting early shock.

To date,these studies of OCT in the ICU patients are rarely. No one has quantified OCT to CI, DO2I、ScvO2.

This study explored:

  1. relationship between patient factors, hemodynamic variables, PtO2, and OCT to mortality;
  2. relationship between PtO2 index, tissue oxygen index, oxygen Challenge index to CI, DO2, ScvO2.

Full description

PtO2 index = PtO2/PaO2;tissue oxygen index=PtO2/FiO2;

5min OCT value = challenged 5minPtO2 - PtO2baseline;

10min OCT value= challenged 10minPtO2- PtO2baseline;

oxygen challenge index = (10minPtO2- PtO2baseline)/(10minPaO2-PaO2baseline)

Enrollment

60 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Requiring a artery catheters, and pulmonary artery catheters or PiCCO-plus or central venous catheters
  • FiO2<80% and SpO2>92%
  • Consent informed

Exclusion criteria

  • Not expected to live

Trial design

60 participants in 1 patient group

Survivor Nonsurvivor

Trial contacts and locations

1

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Central trial contact

huaiwu he; dawei liu, MD

Data sourced from clinicaltrials.gov

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