Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- High energy closed extremity fracture
- Provision of informed consent
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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
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