Overview
The purpose of this research is to test an investigational device called SimPull to see if it is a more efficient method of transferring a patient from one bed to another compared to that of current methods. The purpose of this research is to gather information on the safety and effectiveness of the SimPull device.
Eligibility
Inclusion Criteria:
- Patients requiring lateral transfer for an invasive cardiac procedure to and from gurney to exam table.
- Patients requiring lateral transfer for an invasive cardiac procedure to and from exam table to gurney.
- Patient does not have compound fractures or cervical fractures present.
- Patient does not have skin damage or open wounds to the dorsal cavity.
- Patient or legally authorized representative (LAR) must be able/present to sign consent.
Exclusion Criteria:
- Patients who do not require lateral transfer for an invasive cardiac procedure to and from gurney to exam table.
- Patients who do not require lateral transfer for an invasive cardiac procedure to and from exam table to gurney.
- Patient has compound fractures or cervical fractures present.
- Patient has skin damage or open wounds to the dorsal cavity.
- Patient or legally authorized representative (LAR) are unable/present to sign consent.