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

Assessment of Transcutaneous Oxygen Tension and Oxygen Challenge Test in Adult Intensive Care Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01174966
Acronym
ICUPtO2OCT
Enrollment
60
Registered
2010-08-04
Start date
2009-09-30
Completion date
2010-10-31
Last updated
2010-08-04

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

Conditions

Sepsis, Shock

Keywords

oxygen challenge test, shock, mortality, Oxygen Delivery Index, cardiac output index

Brief summary

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.

Detailed 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)

Interventions

None listed

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 95 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
ICU mortality28 day after enrollmented

Secondary

MeasureTime frame
hospital mortality28 day after enrollmented

Countries

China

Contacts

Primary Contactdawei liu, MD
dwliu98@yahoo.com010-65296091
Backup Contacthuaiwu he
tjmuhhw@hotmail.com010-65296094

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026