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A Study to Evaluate SimPull for Lateral Patient Transfer

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Mayo Clinic

Status

Completed

Conditions

Lateral Patient Transfer

Treatments

Device: SimPull Lateral Transfer Device
Other: Survey

Study type

Interventional

Funder types

Other

Identifiers

NCT05856123
22-004929

Details and patient eligibility

About

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.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 3 patient groups

Group 1: Standard of Care Transfer
No Intervention group
Description:
After cardiac catheterization lab or electrophysiology lab procedure, the subject will be moved from one bed to another using the current standard of practice lateral patient transfer methods by nursing staff.
Group 2: SimPull Device Transfer
Experimental group
Description:
After cardiac catheterization lab or electrophysiology lab procedure, the subject will be moved from one bed to another using the SimPull device.
Treatment:
Device: SimPull Lateral Transfer Device
Group 3: Clinicians
Active Comparator group
Description:
Study clinicians complete a survey after conducting intervention or standard of care on participants.
Treatment:
Other: Survey

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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