Noninvasive Cardiac Output Monitoring in Pulmonary Hypertension



Status:Active, not recruiting
Conditions:High Blood Pressure (Hypertension), High Blood Pressure (Hypertension)
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:4/6/2019
Start Date:November 2016

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Comparison of noninvasive cardiac output monitoring device with Fick and thermodilution
methods during right heart catheterization in patients with pulmonary hypertension.


Inclusion criteria:

- Age > 18 years

- Diagnosis of Group 1 or Group 4 PAH based on PAPm > 25 mmHg, PAWP <15 mmHg, PVR >3 WU
and consistent clinical history. Note: for logistical reasons, patients at high
suspicion for Group 1 or Group 4 PAH will sign informed consent to have the NICOM
device applied during right heart catheterization before the procedure; if it is found
that the patient does not meet the definition of Group 1 or Group 4 PAH during right
heart catheterization, he/she will be excluded.

- Willingness and ability to comply with study procedures.

- No known hypersensitivity to the components of NICOM electrodes

Exclusion criteria:

- Unwillingness to sign informed consent or inability or unwillingness to comply with
study procedures

- Evidence of postcapillary pulmonary hypertension on right heart catheterization
We found this trial at
1
site
Santa Barbara, California 93105
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mi
from
Santa Barbara, CA
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