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LIFT Home Study of Non-Invasive ARC Therapy for Spinal Cord Injury

NCT05284201 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2022-09-16

No results posted yet for this study

Summary

The LIFT Home Study is an observational, single-arm study designed to assess the safety of non-invasive electrical spinal stimulation (ARC Therapy) administered by the LIFT System to treat upper extremity functional deficits in people with chronic tetraplegia.

Conditions

  • Chronic Spinal Cord Injury

Interventions

DEVICE

LIFT System

The LIFT System delivers the Functional task practice and ARC Therapy to improve upper extremity function in individuals with tetraplegia.

Sponsors & Collaborators

  • ONWARD Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Candace Tefertiller, PT, DPT, PhD, NCS · Craig Hospital, Colorado, United States

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
22 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-03
Primary Completion
2022-06-30
Completion
2022-09-13
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT05284201 on ClinicalTrials.gov