Comparison of Noninvasive vs. Invasive Hemodynamic Measurements
Running, not enrolling
Conditions studied: Heart Failure, Congestive
In brief
Comparison of a non-invasive method of measuring central venous pressure to the conventional modality of invasive central venous pressure.
Key facts
- Study ID
- NCT06689215
- Run by
- Nihon Kohden
- People needed
- 30
- Starts
- 2024-10-21
- Expected to finish
- 2027-03-30
- Last updated by the study team
- 2026-02-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult age over 18 years.
- Arm circumference is 18 cm to 55 cm
- Subject will have an existing indwelling central venous catheter during their ICU stay
- Subject or legally authorized representative (LAR) is able to understand the risks and potential benefits of participating in the study and is willing to provide written informed consent
- Subject or LAR is willing and able to comply with protocol procedures
You may not qualify if…
- Finger and/or upper arm anatomical anomaly or disease that may interfere with attaching a pulse oximeter sensor and/or blood pressure cuff.
- Pregnant (self-reported)
- Upper extremity deep venous thrombosis currently being treated
- Severe skin disease involving the upper arm(s)
- Study investigator may exclude patients based on clinical judgement
Where it is running
- Stanford University Hospital — Stanford, California, United States
Full record on ClinicalTrials.gov
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