Reliability of Central Venous Pressure Measurements
Stopped early · Not applicable
Conditions studied: Hemodynamics, Central Venous Pressure
In brief
The purpose of this study is to compare CVP measurements from CICCs and PICCs. The investigators will also evaluate whether or not the duration of CICC placement affects the differences in CVP measurements between the CICCs and PICCs. The investigators hypothesize that the differences between the CVP measurements of the CICCs and PICCs will be clinically insignificant.
Key facts
- Study ID
- NCT01116973
- Run by
- University of Oklahoma
- People needed
- 17
- Starts
- 2009-09-02
- Expected to finish
- 2016-08-27
- Last updated by the study team
- 2017-05-04
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subject's ability to lay in a supine position with their hands at their sides during CVP measurements
- A consent form signed by the patient or patient's representative
- Subjects that are age 18-90
- Subjects that have an indwelling CICC and are transitioning to a PICC for long-term IV access
- CICC placed in the internal jugular vein or subclavian vein position
You may not qualify if…
- Inability to obtain consent
- Subjects under 18 years of age
- Non-English speaking subjects
- Subjects that are unable to lay flat due to pulmonary complications, increased intracranial pressure (ICP), or unstable spinal cord injuries
- Subjects with known cardiac abnormalities (atrial septal defects or ventricular septal defects, severe tricuspid valve disease, severe pulmonary hypertension, Ejection fraction < 15%)
- Prisoners
- Subjects with known upper extremity deep vein thromboses (subclavian or distal)
- Subjects with non-functional CICC or PICC distal ports
- Subjects with femoral CICCs
- Pregnant women
Where it is running
- Univeristy of Oklahoma Health Sciences Center Dept. Anesthesiology — Oklahoma City, Oklahoma, United States
- Univeristy of Oklahoma Health Sciences Center — Oklahoma City, Oklahoma, United States
Full record on ClinicalTrials.gov
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