Comparison of Hemodynamic Variables Between Using Conventional Invasive Catheter Monitoring and Non-invasive Piezoelectric Sensor

ConditionMonitoring

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age19+

SponsorSMG-SNU Boramae Medical Center

About this trial

Arterial pressure is obtained from invasive arterial monitoring and noninvasive arterial monitoring using piezoelectric sensor and compared.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Cases who require Invasive arterial pressure monitoring d/t bleeding.

Disqualifiers

Patients with cardiovascular disease, cerebrovascular diseases, renal disease, or Marfan syndrome

Pregnancy

Trial design

Design model

Crossover

Treatments tested in this trial

Arterial pressure monitoring
Other intervention
Arterial pressure is monitored and obtained

Treatment groups

30 Participants

are divided into 2 treatment groups

Group A: Invasive groupActive comparator 1 intervention

Group B: Noninvasive arterial monitoringExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Arterial pressure

After the induction of anesthesia, 20G catheter is placed for invasive arterial pressure monitoring in the radial artery and pressure sensor is attached for noninvasive arterial pressure monitoring in the contralateral radial artery. Then, invasive and noninvasive arterial pressures are monitored and obtained simultaneously.

Time frame

For 30 min after the induction of anesthesia,

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

SMG-SNU Boramae Medical Center

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: