Comparison of Nasal and Forehead Oximetry in Critically Ill Patients at Risk for Decreased Peripheral Perfusion
Completed · Not applicable
Conditions studied: Hypotension, Pressure Ulcer
In brief
Continuous pulse oximetry monitoring is the standard of care in critically ill patients in emergency departments, operating rooms and intensive care units. In patients with poor peripheral perfusion (low blood flow) due to peripheral vascular disease, low body temperature, or shock and the use of medications to raise the blood pressure, clinicians have difficulty obtaining an accurate measurement. This study compares the accuracy of forehead oximetry sensors to nasal alar sensors to lab oximetry measures and on the rate of device related pressure ulcers with both.
Key facts
- Study ID
- NCT02382133
- Run by
- Washington University School of Medicine
- People needed
- 43
- Starts
- 2014-10-01
- Expected to finish
- 2016-09-01
- Last updated by the study team
- 2017-06-07
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Presence of an existing arterial catheter for blood sampling and one of the following:
- Difficulty obtaining a consistent signal from a digit or ear sensor or
- On pressors of at least 0 .10 mcg/kg/min of norepinephrine or
- Core temperature < or equal to 35 degrees C
You may not qualify if…
- Anatomic impediments (burns, wounds, dressings, etc.) to placement of the sensor on the forehead or nasal alar
- History of known dyshemoglobinemias evidenced by carboxyhemoglobin levels > 10% or methemoglobin level > 2%
- Severe anemia with hemoglobin < 5 g/dL
- Pregnant women
Where it is running
- Barnes-Jewish Hospital at Washington University — St Louis, Missouri, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.