HSI: Investigation of the Use of Hyperspectral Imaging in Foot Surgery Patients

Sponsor
University of Texas Southwestern Medical Center (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03787862
Collaborator
3M (Industry)
0
2
12
0
0

Study Details

Study Description

Brief Summary

To investigate novel advanced imaging techniques (hyperspectral imaging) that could enable clinicians to determine the degree and effectiveness of blood flow to tissues during surgery.

There are a number of disorders where blood flow is inadequate to provide nutrients and oxygen to tissues. Under some circumstances, surgery is required to either improve the blood flow or remove tissues that are poorly perfused. In other cases, occlusion of the blood supply to an organ is temporarily or permanently performed to minimize blood loss during a surgical procedure.

Additionally, there are disorders where the location of certain blood containing structures is important but not immediately obvious to surgeons during an operation. Knowledge of where those structures are is very important and could greatly improve the safety of various surgical procedures.

Patients of the investigator who are scheduled for foot surgery will be provided the opportunity to participate in this research. After giving informed consent, hyperspectral images will be obtained at various points during the surgical procedure.

As this technology is non-invasive, it is not expected to interfere with or change the procedure they are undergoing. Once the surgical procedure is complete, imaging will be saved to a disk for later evaluation.

100 subjects will participate in this study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The hyperspectral imager will be turned on at various time points during surgery, to measure the spectral wavelengths of tissues. The surgery being performed will in no way be altered by the imaging device and post surgical follow-up of patients will be standard of care appropriate to the surgical procedure.

    Patients will have HSI performed only during their surgery. They will not receive additional medications and will have no additional follow up. Participating in this study will not add extra appointments, procedures, or time requirements for the patient. The patient's medical record may be referenced for information after the surgery for up to one year. There are no costs to the patient for participation in this study.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    0 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Investigation of the Use of Hyperspectral Imaging in Foot Surgery Patients
    Anticipated Study Start Date :
    Jun 13, 2014
    Anticipated Primary Completion Date :
    Jun 13, 2014
    Actual Study Completion Date :
    Jun 13, 2015

    Arms and Interventions

    Arm Intervention/Treatment
    Hyperspectral Imaging (HSI)

    Patients scheduled for foot surgery will be imaged using the HSI device. Data will be gathered from the electronic medical record for one year to determines the outcomes of the surgery, any complications, re-hosptializations, re-ulcerations or amputation.

    Outcome Measures

    Primary Outcome Measures

    1. Correlation of HSI images with patient outcomes [1 year]

      Patient video images will be correlated with individual outcomes. Patients undergoing similar procedures will then be compared in terms of surgical outcome and differences in hyperspectral imaging variables.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male and female patients

    • 18 years or older undergoing foot surgery

    • Speak and read English or Spanish.

    • Able to provide written informed consent.

    Exclusion Criteria:
    • Patients unable to give written informed consent

    • Patients who cannot speak and read English or Spanish will be excluded.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Parkland Health and Hospital System Dallas Texas United States 75390
    2 UT Southwestern Medical Center Dallas Texas United States 75390

    Sponsors and Collaborators

    • University of Texas Southwestern Medical Center
    • 3M

    Investigators

    • Principal Investigator: Lawrence A Lavery, DPM, MPH, UT Southwestern Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Texas Southwestern Medical Center
    ClinicalTrials.gov Identifier:
    NCT03787862
    Other Study ID Numbers:
    • HSI in Foot Surgery
    First Posted:
    Dec 26, 2018
    Last Update Posted:
    Dec 26, 2018
    Last Verified:
    Dec 1, 2018
    Keywords provided by University of Texas Southwestern Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 26, 2018