3D-printed Bone Models in Addition to CT Imaging for Intra-articular Fracture Repair (SPRINT)
Primary Purpose
Distal Humerus Fracture, Distal Femur Fracture, Distal Tibia Fracture
Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
3D printed (3DP) bone models + CT imaging
CT imaging
Sponsored by
About this trial
This is an interventional treatment trial for Distal Humerus Fracture focused on measuring 3D Printing, Intra-articular Fracture, Patient-specific instrumentation
Eligibility Criteria
Inclusion Criteria:
- age 18 years or older
- with intra-articular fracture of the proximal or distal humerus, proximal ulna, proximal radius, distal femur, or proximal or distal tibia (pilon fracture)
- requiring anticipated surgical repair of fracture
- with pre-operative CT scan already available as part of routine assessment
Exclusion Criteria:
- pathological fracture
- multiple fractures requiring simultaneous or staged operations
- fractures around the hip, pelvis and acetabulum, and any other fracture types not specified in the inclusion criteria
- requiring surgery within 24 hours of admission
- unable or unwilling to give consent to participate
Sites / Locations
- Queen Mary Hospital, The University of Hong KongRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
3D-printed models plus CT imaging
CT imaging alone
Arm Description
Fracture repair surgery using sterilized 3DP models, CT-MPR and CT-3DR for planning and intraoperative visualization
Fracture repair surgery using CT-MPR and CT-3DR for planning and intraoperative visualization
Outcomes
Primary Outcome Measures
Quality of articular surface reduction grading assessed by three-point scale
The quality of articular surface reduction will be rated by two surgeons blinded to intervention allotment assessing post-operative and intraoperative fluoroscopic images. The Kappa value will be recorded for inter-observer agreement between two observers (1. Perfect reduction, 2. Observable imperfections 1-2mm, 3. Significant imperfections >2mm)
Skin to skin duration of surgery (minutes)
The skin to skin duration of the surgery will be recorded.
Secondary Outcome Measures
Total fluoroscopy time (seconds)
The total intraoperative fluoroscopy time will be recorded in seconds.
Intraoperative blood loss (mL)
The patient's blood loss during the surgery will be recorded.
Total length of skin incision (mm)
The total length on the incision will be measured post operation.
Total tourniquet time (minutes)
Total time the tourniquet was applied will be recorded.
Incidence of surgical complications
Incidence of infection, neurological deficit, wound breakdown, loss of fixation, revision surgery will be recorded at follow up.
Quality of articular surface reduction grading assessed by three-point scale
The quality of articular surface reduction will be rated by two surgeons blinded to intervention allotment assessing post-operative and intraoperative fluoroscopic images. The Kappa value will be recorded for inter-observer agreement between two observers (1. Perfect reduction, 2. Observable imperfections 1-2mm, 3. Significant imperfections >2mm)
Health-related quality of life measured by SF-12 Chinese (HK) version
12-item Short Form Health Survey (SF-12), a patient-reported outcome measure of HRQOL comprised of a mental component (MCS) and physical component (PCS), each with a final score ranging from 0 (worst outcome) to 100 (best outcome).
Full Information
NCT ID
NCT04748016
First Posted
February 5, 2021
Last Updated
July 19, 2022
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04748016
Brief Title
3D-printed Bone Models in Addition to CT Imaging for Intra-articular Fracture Repair
Acronym
SPRINT
Official Title
Sterilised 3D-PRINTed Bone Models in Addition to Conventional CT Imaging for Operative Visualisation in Complex Intra-articular Fracture Repair - A Multi-centre, Double-blind Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 13, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to compare the effectiveness of 3D-printed bone models in addition to CT imaging versus CT imaging alone on surgical quality and operation time for patients undergoing surgical repair of intra-articular fractures.
Detailed Description
Surgical fixation of intra-articular fractures is a technically demanding task that poses significant challenges to orthopaedic surgeons. Articular fragments may be comminuted, depressed, or impacted, and neighbouring soft tissue is often heavily compromised. Furthermore, aggressive surgical dissection is typically necessary to achieve adequate visualisation, and anatomical reduction often devitalises bone fragments and invites deep infection. The management of intra-articular fractures requires a well-designed preoperative plan and a skilfully executed surgical tactic to guarantee the best possible outcome. Multiplanar reformation (CT-MPR) and three-dimensional reconstruction (CT-3DR) are imaging techniques that have enhanced intraoperative visualisation, however, accurate analysis of complex fractures remains challenging.
3D printing is a rapidly developing, low-cost technology that is already being applied across numerous contexts in orthopaedics and traumatology. 3D printed bone models can be produced from digitised CT data in a matter of hours, providing a dimensionally accurate representation of the patient's skeleton which approximates real-life visual and tactile experiences. When used in preoperative planning, these models have shown to improve surgeon communication and shorten surgical duration. Despite positive early results, few clinical studies have studied the effect of 3D bone model use on surgical outcome. The purpose of this randomised controlled trial is to compare the effectiveness of intraoperatively utilised 3D bone models in addition to conventional CT imaging on reduction quality and surgical duration versus CT imaging alone for patients undergoing surgical fixation of complex intraarticular fractures.
Patients providing informed consent will be screened for eligibility. All eligible patients will be randomly assigned in a double-blind manner (participant and outcome assessor) to receive surgical fracture fixation with or without the addition of sterilised 3D-printed bone models to standard CT imaging for intraoperative visualisation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Distal Humerus Fracture, Distal Femur Fracture, Distal Tibia Fracture, Proximal Humeral Fracture
Keywords
3D Printing, Intra-articular Fracture, Patient-specific instrumentation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Double-blind randomised control trial with 40 patients in two interventional arm
Masking
ParticipantOutcomes Assessor
Masking Description
Participants are randomly assigned to either one of the interventional arm and will not be informed of the randomisation result.
A blinded reviewer will assess the postoperative radiographs and surgical quality.
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
3D-printed models plus CT imaging
Arm Type
Experimental
Arm Description
Fracture repair surgery using sterilized 3DP models, CT-MPR and CT-3DR for planning and intraoperative visualization
Arm Title
CT imaging alone
Arm Type
Active Comparator
Arm Description
Fracture repair surgery using CT-MPR and CT-3DR for planning and intraoperative visualization
Intervention Type
Other
Intervention Name(s)
3D printed (3DP) bone models + CT imaging
Intervention Description
In addition to CT-MPR and CT-3DR, 3DP models will be used for surgical planning and intraoperative visualization.
Intervention Type
Other
Intervention Name(s)
CT imaging
Intervention Description
CT-MPR and CT-3DR used for surgical planning and intraoperative visualization.
Primary Outcome Measure Information:
Title
Quality of articular surface reduction grading assessed by three-point scale
Description
The quality of articular surface reduction will be rated by two surgeons blinded to intervention allotment assessing post-operative and intraoperative fluoroscopic images. The Kappa value will be recorded for inter-observer agreement between two observers (1. Perfect reduction, 2. Observable imperfections 1-2mm, 3. Significant imperfections >2mm)
Time Frame
Immediately post-operation
Title
Skin to skin duration of surgery (minutes)
Description
The skin to skin duration of the surgery will be recorded.
Time Frame
Immediately post-operation
Secondary Outcome Measure Information:
Title
Total fluoroscopy time (seconds)
Description
The total intraoperative fluoroscopy time will be recorded in seconds.
Time Frame
Immediately post-operation
Title
Intraoperative blood loss (mL)
Description
The patient's blood loss during the surgery will be recorded.
Time Frame
Immediately post-operation
Title
Total length of skin incision (mm)
Description
The total length on the incision will be measured post operation.
Time Frame
Immediately post-operation
Title
Total tourniquet time (minutes)
Description
Total time the tourniquet was applied will be recorded.
Time Frame
Immediately post-operation
Title
Incidence of surgical complications
Description
Incidence of infection, neurological deficit, wound breakdown, loss of fixation, revision surgery will be recorded at follow up.
Time Frame
3 months post-operation
Title
Quality of articular surface reduction grading assessed by three-point scale
Description
The quality of articular surface reduction will be rated by two surgeons blinded to intervention allotment assessing post-operative and intraoperative fluoroscopic images. The Kappa value will be recorded for inter-observer agreement between two observers (1. Perfect reduction, 2. Observable imperfections 1-2mm, 3. Significant imperfections >2mm)
Time Frame
3 months post operation
Title
Health-related quality of life measured by SF-12 Chinese (HK) version
Description
12-item Short Form Health Survey (SF-12), a patient-reported outcome measure of HRQOL comprised of a mental component (MCS) and physical component (PCS), each with a final score ranging from 0 (worst outcome) to 100 (best outcome).
Time Frame
3 months post-operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
age 18 years or older
with intra-articular fracture of the proximal or distal humerus, proximal ulna, proximal radius, distal femur, or proximal or distal tibia (pilon fracture)
requiring anticipated surgical repair of fracture
with pre-operative CT scan already available as part of routine assessment
Exclusion Criteria:
pathological fracture
multiple fractures requiring simultaneous or staged operations
fractures around the hip, pelvis and acetabulum, and any other fracture types not specified in the inclusion criteria
requiring surgery within 24 hours of admission
unable or unwilling to give consent to participate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christian Fang
Phone
22554581
Email
cfang@hku.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Fang
Organizational Affiliation
Dept of Orthopaedics and Traumatology, Queen Mary Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Mary Hospital, The University of Hong Kong
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christian Xinshuo Fang
Phone
22554581
First Name & Middle Initial & Last Name & Degree
Christian Xinshuo Fang
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Anonymized dataset to be included as supplementary data in final publication
IPD Sharing Time Frame
Within 1 year of study completion
IPD Sharing Access Criteria
Additional information available upon reasonable request of principal investigator
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3D-printed Bone Models in Addition to CT Imaging for Intra-articular Fracture Repair
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