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

About this trial
This is an interventional treatment trial for Bone Fracture
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
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
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
We'll reach out to this number within 24 hrs