Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06858488

A Pilot Study on the Technical Feasibility of an Electrical Impedance Tomography Device for Soft Tissue Injury Following High Energy Extremity Fractures

Led by Dartmouth-Hitchcock Medical Center · Updated on 2025-06-22

30

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

D

Dartmouth-Hitchcock Medical Center

Lead Sponsor

D

Dartmouth College

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to evaluate the use of an electrical impedance tomography (EIT) device in patients who have experienced high-energy extremity trauma. The study focuses on assessing the technical feasibility of the EIT system for imaging soft tissue injuries following high-energy closed extremity fractures. Patients aged 18 and older with these types of fractures will be enrolled to better understand how the device performs in clinical settings. Participants will undergo imaging with the EIT device in several hospital locations including the Emergency Department, Operating Room, Orthopaedic Clinic, and inpatient hospital rooms. The study involves patients receiving extremity surgery related to their fractures. The procedure is designed to capture data on the soft tissue injury using the EIT device, with a focus on the feasibility and acceptability of using this technology. During the study, researchers will monitor how well the EIT device works within a 20-minute imaging session. Participants will be evaluated across different hospital settings to gather information on the device's practical use. The study is led by Dartmouth-Hitchcock Medical Center and will continue until June 2027. Participant involvement includes undergoing the imaging procedure and providing consent, with no mention of long-term follow-up or additional interventions.

CONDITIONS

Brief Title

Bioimpedance for Ortho Trauma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • High energy closed extremity fracture
  • Provision of informed consent
Not Eligible

You will not qualify if you...

  • Metatarsal fractures
  • Injury to both lower extremities precluding contralateral imaging
  • Presence of an implanted electronic device (e.g. pacemaker, vagal stimulator, deep brain stimulator) or electrodes or electrical wires
  • Currently pregnant, potentially pregnant, or lactating women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Up to several days

Participants undergo surgery for their extremity fracture and receive immediate post-operative care.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Dartmouth-Hitchcock Medical Center

Lebanon, New Hampshire, United States, 03756

Actively Recruiting

Loading map...

Research Team

H

Holly B Symonds

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

Similar Trials

Managing Symptoms and Disability After Traumatic Injury Usin...

Trauma Injury

Actively Recruiting

1 location

Hematopoietic Stem Cell Dysfunction in the Elderly After Sev...

Trauma Injury

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here