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CPR clinical trials

View clinical trials related to CPR.

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NCT ID: NCT03065647 Completed - Cardiac Arrest Clinical Trials

ECPR for Refractory Out-Of-Hospital Cardiac Arrest

EROCA
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

In the U.S. alone, over 300,000 people per year have sudden out-of-hospital cardiac arrest (OHCA), and less than 1 out of 10 survive. The current standard practice for treating OHCA is to perform cardiopulmonary resuscitation (CPR) and Advanced Cardiovascular Life Support (ACLS) at the scene until either the heart is restarted or resuscitation efforts are considered hopeless and discontinued. An alternative strategy for those with refractory OHCA is expedited transport with ongoing mechanical CPR to an Emergency Department capable of performing extracorporeal cardiopulmonary resuscitation (ECPR). The purpose of study is to test if this strategy is feasible and beneficial.

NCT ID: NCT01117883 Completed - Cardiac Arrest Clinical Trials

Sternal Wall Pressure in the Cath Lab

Start date: April 2010
Phase: N/A
Study type: Interventional

This protocol is a prospective interventional pilot study at the Children's Hospital of Philadelphia to determine whether or not two increments of sternal pressure known to occur during "leaning" in CPR affects hemodynamic function, coronary perfusion pressures, and intrathoracic pressure in order to inform the resuscitation community on reasonable target pressures to avoid "leaning" on the chest during pediatric CPR.

NCT ID: NCT00630773 Completed - CPR Clinical Trials

Q-CPR Compression Sensor Size Qualification in Children

PUCK
Start date: March 2007
Phase: N/A
Study type: Observational

This prospective, pilot observational study will be performed in the Emergency Department (ED), Pediatric Intensive Care Unit (PICU), Operating Room (OR) and regular inpatient care area (RIPCA) settings at the Children's Hospital of Philadelphia. The differences in trained pediatric health care provider placement of the compression sensor and their assessment of the suitability / willingness to use the current or size modified sensor will be assessed.