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Digital Three-dimensional Imaging Models for Repair of Complex Long Bone Fractures

Primary Purpose

Bone Fracture

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
CT scan for internal fixation
conventional internal fixation
Sponsored by
Qinghai University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bone Fracture

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Long bone fractures in the four limbs, such as middle segment of humerus, femur, ulna, radius, tibia and fibula; fractures are not related to the articular surface
  • Diagnosed with complex long bone fractures via X-ray
  • Admission within 6 hours after injury

Exclusion Criteria:

  • Pathological fractures with vascular and nerve injuries
  • Split fractures of the humeral head
  • Neer IV fractures
  • Humeral head compression area greater than 40%
  • Glenohumeral dislocation
  • Conscious disturbance, cerebral infarction, tumor, serious medical complications, such as heart, lung, kidney failure, severe hypertension, diabetes and blood diseases
  • History of elbow joint dysfunction or shoulder joint disease
  • Unwilling to sign the informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    the observation group

    the control group

    Arm Description

    32 patients with complex long bone fractures will be randomized to undergo digital three-dimensional models will be established by CT scan for internal fixation in the observation group.

    31 patients will be randomized to undergo conventional internal fixation in the control group.

    Outcomes

    Primary Outcome Measures

    X-ray examination
    To evaluate total efficacy at postoperative 6 months

    Secondary Outcome Measures

    Harris scores
    To assesse the recovery of hip function
    Visual Analogue Scale
    To evaluate the pain, and the high score represents severe pain.

    Full Information

    First Posted
    November 12, 2016
    Last Updated
    February 7, 2018
    Sponsor
    Qinghai University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02964754
    Brief Title
    Digital Three-dimensional Imaging Models for Repair of Complex Long Bone Fractures
    Official Title
    Digital Three-dimensional Imaging Models for Repair of Complex Long Bone Fractures: a Randomized Controlled Trial With 6-month Follow-up
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2014 (undefined)
    Primary Completion Date
    April 2016 (Actual)
    Study Completion Date
    December 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Qinghai University

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    To verify whether digital three-dimensional model-assisted internal fixation can obtain better effects in the repair of complex long bone fractures compared with conventional internal fixation.
    Detailed Description
    History and current related studies The internal fixator is difficult to completely fit the bone surface at the site of complex long bone fracture, which reduces the firmness of fixation. From a safety point of view, the establishment of a digital three-dimensional measurement model is undoubtedly a very reliable and intuitive way. Digital three-dimensional models are established after CT scan, and these models can greatly reflect the site and degree of fractures, and reduce anatomical parameters, with high degree of simulation and feasibility. Adverse events The investigators will record adverse events, including screw loosening and falling off, steel plate fracture and bending, joint stiffness, delayed healing or non-healing, peripheral nerve injury and infection. If severe adverse events occur, investigators will report details, including the date of occurrence and measures taken to treat the adverse events, to the principle investigator and the institutional review board within 24 hours. Data collection, management, analysis and open-access Data collection: Case report forms with demographic data, disease diagnosis, accompanying diseases, drug allergy history, and adverse events will be collected, processed using Epidata software (Epidata Association, Odense, Denmark), collated, and then recorded electronically by data managers using a double-data entry strategy. Data management: The locked electronic database will be accessible and locked only by the project manager, and will not be altered. All data regarding this trial will be preserved by the Affiliated Hospital of Qinghai University, China. Data analysis: The electronic database will be statistically analyzed by a professional statistician who will create an outcome analysis report that will be submitted to the lead researchers. An independent data monitoring committee will supervise and manage the trial data, ensuring a scientific and stringent trial to yield accurate and complete data. Data open access: Anonymized trial data will be published at www.figshare.com. Statistical analysis Statistical analysis will be performed using SPSS 19.0 software, and will follow the intention-to-treat principle. Normally distributed measurement data will be expressed as mean ± standard deviation, and minimums and maximums. Non-normally distributed measurement data will be expressed as lower quartile (q1), and median and upper quartile (q3). Fisher's exact test will be performed for comparison of total efficacy and the incidence of adverse reactions preoperatively and 6 months postoperatively. Mann Whitney U test will be used to compare Harris score, Visual Analogue Scale, operation time and hospital stay between the two groups. The significance level will be α = 0.05.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bone Fracture

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    63 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    the observation group
    Arm Type
    Experimental
    Arm Description
    32 patients with complex long bone fractures will be randomized to undergo digital three-dimensional models will be established by CT scan for internal fixation in the observation group.
    Arm Title
    the control group
    Arm Type
    Experimental
    Arm Description
    31 patients will be randomized to undergo conventional internal fixation in the control group.
    Intervention Type
    Device
    Intervention Name(s)
    CT scan for internal fixation
    Intervention Description
    In the observation group, digital three-dimensional models will be established by CT scan for internal fixation.
    Intervention Type
    Procedure
    Intervention Name(s)
    conventional internal fixation
    Intervention Description
    In the control group, patients will undergo conventional internal fixation.
    Primary Outcome Measure Information:
    Title
    X-ray examination
    Description
    To evaluate total efficacy at postoperative 6 months
    Time Frame
    postoperative 6 months
    Secondary Outcome Measure Information:
    Title
    Harris scores
    Description
    To assesse the recovery of hip function
    Time Frame
    preoperatively and 6 months postoperatively
    Title
    Visual Analogue Scale
    Description
    To evaluate the pain, and the high score represents severe pain.
    Time Frame
    preoperatively and 6 months postoperatively

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Long bone fractures in the four limbs, such as middle segment of humerus, femur, ulna, radius, tibia and fibula; fractures are not related to the articular surface Diagnosed with complex long bone fractures via X-ray Admission within 6 hours after injury Exclusion Criteria: Pathological fractures with vascular and nerve injuries Split fractures of the humeral head Neer IV fractures Humeral head compression area greater than 40% Glenohumeral dislocation Conscious disturbance, cerebral infarction, tumor, serious medical complications, such as heart, lung, kidney failure, severe hypertension, diabetes and blood diseases History of elbow joint dysfunction or shoulder joint disease Unwilling to sign the informed consent
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Zichun Zhao, Master
    Organizational Affiliation
    Affiliated Hospital of Qinghai University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Digital Three-dimensional Imaging Models for Repair of Complex Long Bone Fractures

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