Feasibility of an Electrical Impedance Tomography Device for Pulmonary Function Testing in ALS Patients

NCT05287958 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 58

Last updated 2024-04-16

No results posted yet for this study

Summary

This is an unblinded pilot study to investigate the technical feasibility of using an electrical impedance tomography device for noninvasive pulmonary function monitoring in ALS patients. The study will enroll patients with ALS in one cohort and healthy volunteers in a second cohort that will both undergo EIT imaging with the investigational device prior to and while performing a standard PFT procedure.

Conditions

Interventions

DIAGNOSTIC_TEST

EIT

EIT comprises a chest belt that is connected to a computer via a universal serial bus (USB) or an Ethernet cable. The chest belt captures EIT data, which is transmitted via the USB or Ethernet cable to the computer. Tomography-like impedance images of the lungs are computed and displayed on the computer. The impedance images will be used to evaluate lung recruitment and other pulmonary function parameters that are currently measured using standard-of-care PFT devices.

Sponsors & Collaborators

  • Dartmouth-Hitchcock Medical Center

    collaborator OTHER
  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH
  • Beth Israel Deaconess Medical Center

    lead OTHER

Principal Investigators

  • Seward Rutkove, MD · Beth Israel Deaconess Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-07-15
Primary Completion
2023-09-20
Completion
2023-09-20

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT05287958 on ClinicalTrials.gov