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RECRUITING
NCT05928052
NA

Spinal Cord Stimulation to Shorten Ventilator Dependence in ARDS Patients

Sponsor: University of California, Los Angeles

View on ClinicalTrials.gov

Summary

This is an early phase, proof-of-concept clinical trial assessing the safety and feasibility of non-invasive spinal cord stimulation to prevent respiratory muscle atrophy in mechanically ventilated ARDS patients. The investigators will recruit 10 elective surgery patients (surgery cohort) and 10 ARDS patients (ARDS cohort) for this study. A non-invasive, alpha-prototype Restore Technology stimulator using hydrogel surface electrodes will be used to stimulate the spinal cord at the cervical or thoracic level.

Official title: Transcutaneous Spinal Cord Stimulation to Improve Respiratory Function and Shorten Ventilator Dependence in Patients with ARDS

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2023-04-18

Completion Date

2029-01-06

Last Updated

2025-03-10

Healthy Volunteers

No

Interventions

DEVICE

Transcutaneous Biopac Electrical Stimulator

A transcutaneous electrical stimulator sends low levels of electrical current through surface hydrogel electrodes directly to the spinal cord to improve function.

Locations (1)

University of California, Los Angeles

Los Angeles, California, United States