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Arterial Line clinical trials

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NCT ID: NCT06383000 Not yet recruiting - Blood Pressure Clinical Trials

Assessment of Effectiveness of Continuous Non-invasive Haemodynamic Monitor by Compared to Invasive Blood Pressure and Pulse Oximeter Monitoring on Patients Undergoing General Anesthesia Surgeries for More Than 60 Minutes

Start date: June 1, 2024
Phase:
Study type: Observational

The goal of this observational study is to assess whether the continuous non-invasive haemodynamic monitor MOH200 (measuring blood pressure as well as pulse rate) is effective or not in people undergoing general anesthetic surgeries for more than 60 minutes with planned invasive blood pressure and pulse oximeter monitoring. Researchers will compare blood pressure data derived from MOH200 to the invasive blood pressure (IBP) data to see if the MOH200 is effective to measure the blood pressure of a surgical person. Also, researchers will compare pulse rate data drived from MOH200 to that from the pulse oximeter to see if the MOH200 is effective to measure the pulse rate of a surgical person. Participants will be asked to be applied with MOH200 monitoring while IBP monitoring and pulse oximeter are applied. And after 30 minutes of the surgery, researchers will monitor the adverse effects occurred on the skin of participants to assess the safety of MOH200.

NCT ID: NCT05689294 Completed - Anesthesia Clinical Trials

Non Invasive Continuous Blood Pressure Sensor

Start date: April 1, 2023
Phase:
Study type: Observational

The primary objective of this study is to collect training data in order to establish a method for correlating arterial blood pressure with voltage output signals from a non-invasive piezoelectric array sensor placed on the skin superficial to the radial artery.

NCT ID: NCT05443061 Recruiting - Ischemia Clinical Trials

Subcutaneous Nitroglycerin to Prevent Radial Artery Occlusion in Children

Start date: September 8, 2022
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the vasodilative effect of subcutaneous nitroglycerin to prevent radial arterial occlusion(RAO) after removal of the radial arterial catheter in pediatric patients. The hypothesis of this study is that subcutaneous nitroglycerin will decrease the incidence of radial arterial occlusion after radial arterial catheter removal in pediatric patients by increasing the radial artery size and improving the first-attempt success rate of radial artery cannulation. This is a single-center, double-blind, randomized, placebo-controlled study comparing the effect of subcutaneous nitroglycerin and saline on radial artery cannulation and catheter removal in pediatric patients. Prior to the procedure, each patient will be randomized into either the control arm, saline, or the study arm, nitroglycerin.

NCT ID: NCT05030649 Completed - Arterial Line Clinical Trials

Smart-glasses During the Ultrasound-guided Radial Arterial Catheterization in Pediatric Patients by Trainees

Start date: September 17, 2021
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the effect of smart glasses (Head-mounted display Moverio BT-300 (Epson Inc., USA)) on the first-attempt success rate of radial artery cannulation in pediatric patients by less experienced trainees. This study hypothesizes that the use of smart glasses improves the hand-eye coordination and the first-attempt success rate of radial artery cannulation. This is a single-center, randomized, placebo-controlled study comparing the real-time ultrasound image through smart glasses (intervention group) or the ultrasound machine's monitor (control group) during the radial arterial cannulation in pediatric patients undergoing general anesthesia by less experienced trainees.

NCT ID: NCT04329026 Completed - Arterial Line Clinical Trials

Smart-glasses During the US-guided Radial Arterial Catheterization in Pediatric Patients: a RCT

Start date: April 7, 2020
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the effect of smart glasses (Head-mounted display Moverio BT-300 (Epson Inc., USA)) on the first-attempt success rate of radial artery cannulation in pediatric patients. This study hypothesizes that the use of smart glasses improves the hand-eye coordination and the first-attempt success rate of radial artery cannulation. This is a single-center, randomized, placebo-controlled study comparing the real-time ultrasound image through smart glasses (intervention group) or the ultrasound machine's monitor (control group) during the radial arterial cannulation in pediatric patients undergoing general anesthesia.

NCT ID: NCT03849183 Completed - Arterial Line Clinical Trials

Subcutaneous Nitroglycerin for Pediatric Radial Artery Cannulation

Start date: March 20, 2019
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the vasodilative effect of subcutaneous nitroglycerin during ultrasound-guided radial artery cannulation in pediatric patients. The hypothesis of this study is that the subcutaneous nitroglycerin will increase the radial artery size and improve the first-attempt success rate of radial artery cannulation. This is a single-center, double-blind, randomized, placebo-controlled study comparing the effect of subcutaneous nitroglycerin and saline on radial artery cannulation in pediatric patients undergoing general anesthesia. Prior to the procedure, each patient will be randomized into either the control arm, saline, or study arm, nitroglycerin.

NCT ID: NCT03217019 Completed - Arterial Line Clinical Trials

Guidewire-assisted Radial A-line in Neonate and Infant

Start date: August 7, 2017
Phase: N/A
Study type: Interventional

In neonate and infant, radial artery cannulation may be challenging and multiple attempts are required because of the small diameter. The invastigators will compare the success rates of radial arterial cannulation with a guidewire-assisted technique and the direct technique in pediatric patient(<1yr).

NCT ID: NCT01785654 Not yet recruiting - Adult Patients Clinical Trials

Hemodynamic and Biological Evaluations During Reventilation Collapse in ICU

REVECOL
Start date: March 2013
Phase: N/A
Study type: Observational

Prospective, observational clinical multicentric study in ICU; during the period surrounding the orotracheal intubation.

NCT ID: NCT01702779 Completed - Arterial Line Clinical Trials

Nasal Humidified High Flow Oxygen During Weaning From Mechanical Ventilation : Ultrasonography Study

HiFloLUS
Start date: August 2011
Phase: N/A
Study type: Interventional

This is a prospective, randomized clinical multicentric study in ICU (Intensive Care University)during weaning from mechanical ventilation.

NCT ID: NCT01098773 Completed - Arterial Line Clinical Trials

Pulmonary and Cardiac Ultrasound During Weaning From Mechanical Ventilation

PULCO
Start date: February 2010
Phase: N/A
Study type: Observational

Prospective observational clinical multicentric study in ICU with ventilated patients requiring chest ultrasound analysis.