Detecting Malposition of Trans-pedicle Screw From AP and LAT Plain Radiographs

Sponsor
Taipei Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04784923
Collaborator
(none)
20
4

Study Details

Study Description

Brief Summary

Our study focuses on reducing the use of CT (Computer Tomography) for pedicle screw instrumentation, replacing CT with X-ray. We are writing a program to measure the position on X-ray seeing whether the position meets that on CT after operation. In the future,our method can be used in fluoroscopy, helping us detecting screw malposition efficiently during the surgeries, and hoping reduce complications.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Most of the spine surgeries are decompression, fusion, with instrumentation.Instrumentation needs screws. Pedicle screws are often used. If the pedicle screws are mal-located, that is breaking the pedicle wall; the consequence may be injury of the spinal cord, or nerve root. Some lucky patients may have no symptom; however, broken pedicle will reduce the fixation strength which may reduce fusion rate.

    Detecting malposition screws, currently we use CT (computer tomography) method. The surgeon carefully read the CT slice by slice, looking for clues of screws malposition. However, CT is costly both price and radiation dose.We invented a plain radiograph method which has been pilot tested in one patient with good correction rate. The purpose of this study is to solve the following two clinical problems:

    1. What are the inter-observer and intra-observer reliabilities of CT method?

    2. The radiation dose for CT method is too high. Does our plain radiograph method has the same correction rate? Materials and methods We planned to collect about 100 patients received spinal fusion and instrumentation who has preoperative CT(or MRI) and postoperative plain radiographs and CT. We will firstly verify CT method's reproducibility by interobserver and intra-observer reliability test. With the same databank, we will use our plain radiograph method again, and test if the two methods' results are the same by Chi-square test.

    Conclusion:

    We hope our study can reduce some unnecessary CT examination. In the future,our method can be used in fluoroscopy, helping us detecting screw malposition efficiently during the surgeries, and hoping reduce complications.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    20 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    Detecting Malposition of Trans-pedicle Screw From AP and LAT Plain Radiographs
    Anticipated Study Start Date :
    Mar 1, 2021
    Anticipated Primary Completion Date :
    Jul 1, 2021
    Anticipated Study Completion Date :
    Jul 1, 2021

    Arms and Interventions

    Arm Intervention/Treatment
    Instrumentation patients

    Instrumentation patients

    Outcome Measures

    Primary Outcome Measures

    1. Verify the position of pedicle screw on X-ray compared to that on CT's [30 days]

      Investigators will verify CT method's reproducibility by interobserver and intra-observer reliability test. With the same databank, investigators will use the plain radiograph method again, and test if the two methods' results are the same by Chi-square test.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • s/p pedicle screw insertion surgery

    • good quality postoperative plain radiograph

    • good quality postoperative CT

    Exclusion Criteria:
    • poor quality postoperative plain radiograph

    • poor quality postoperative CT

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Taipei Medical University

    Investigators

    • Study Chair: Chen-Kun Liaw, Taipei Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Taipei Medical University
    ClinicalTrials.gov Identifier:
    NCT04784923
    Other Study ID Numbers:
    • N202007008
    First Posted:
    Mar 5, 2021
    Last Update Posted:
    Mar 5, 2021
    Last Verified:
    Jun 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Mar 5, 2021