MedTrace Logo

Impact of the Erigo Machine on Functional Recovery in ICU Patients

NCT02615990 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2018-05-25

Study results available
· View outcomes & findings →

Summary

This study will assess the effects of the Erigo applied as part of the early mobilization program in the Trauma ICU at the University of Kentucky. It is our hypothesis, that with the Erigo, critically ill patients will tolerate verticalization and mobilization earlier and safely resulting in improved outcomes measured by increased mobility and strength on ICU discharge, decreased requirements for mechanical ventilation, reduced complication rates and decreased ICU and hospital LOS.

Conditions

  • Trauma Patients Requiring Physical Rehabilitation

Interventions

DEVICE

Erigo Pro

Verticalization table with two integrated robotic devices for leg movement and cyclic loading

OTHER

Standard Physical Therapy

Patients receive standard physical therapy.

Sponsors & Collaborators

  • Lisa J. Fryman

    lead OTHER

Principal Investigators

  • Andrew Bernard, MD · University of Kentucky

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2016-11-30
Completion
2016-11-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02615990 on ClinicalTrials.gov