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3D Virtual Planning for Tibial Plateau Fractures

Primary Purpose

Tibial Plateau Fracture

Status
Not yet recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
3D virtual planning software
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Tibial Plateau Fracture

Eligibility Criteria

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

Inclusion Criteria:

• Adult patients of 18 years or older with a tibial plateau fracture who will receive surgical treatment for this fracture

Exclusion Criteria:

  • patients with (general) bone diseases or osseous malformation syndromes,
  • ipsilateral limb fractures,
  • complicated tibial plateau fractures that need an external fixator,
  • previous tibial plateau fractures
  • previous surgical treatment of the tibial plateau

Sites / Locations

  • Massachusetts General Hospital
  • Flinders Medical Center
  • Radboud University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Conventional planning group

3D virtual planning group

Arm Description

Conventional preoperative planning using x-rays and 2D and 3D CT scan

Preoperative planning using x-rays, 2D and 3D CT scans and 3D virtual planning software

Outcomes

Primary Outcome Measures

Duration of surgery
Time in minutes from start of surgery till end of surgery

Secondary Outcome Measures

Blood loss
Amount of blood loss in milliliters during surgery
Surgical complications
Number of complications related to performed surgery or to condition
Perioperative deviations
Number of perioperative deviations of the perioperative plan
Quality of reduction
Postoperative step off in millimeters as measured on postoperative CT scan or X-ray
Quality of reduction
Postoperative gap in millimeters as measured on postoperative CT scan or X-ray
Postoperative knee function
Participant indicated postoperative knee function as measured with the KOOS questionnaire (score between 0 and 100, with 100 being no pain/restrictions in knee function) and SF-36 questionnaire (score between 0 and 100, with 100 being no limitations in social functioning)
Postoperative knee pain
Participant indicated postoperative knee function as measured with the KOOS questionnaire (score between 0 and 100, with 100 being no pain/restrictions in knee function) and SF-36 questionnaire (score between 0 and 100, with 100 being no limitations in social functioning)

Full Information

First Posted
May 10, 2022
Last Updated
May 25, 2022
Sponsor
Radboud University Medical Center
Collaborators
Massachusetts General Hospital, Flinders Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05397327
Brief Title
3D Virtual Planning for Tibial Plateau Fractures
Official Title
Virtual 3D Surgical Planning for Tibial Plateau Fractures: A Multicenter Prospective Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 1, 2022 (Anticipated)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
Massachusetts General Hospital, Flinders Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Tibial plateau fractures are often complex fractures and need a good preoperative planning. The investigators think that a 3D virtual planning software will help the surgeons to get a better understanding of the fracture and therefore want to study the value of 3D virtual planning software in the preoperative planning of tibial plateau fractures. The investigators hypothesize that this software will shorten the duration of surgery, decrease the peroperative bloodloss and the number of complications. Patients with tibial plateau fractures who need surgical treatment will be asked to participate in this study. After participants have given informed consent, they will be randomized between a 'traditional preoperative planning' and a '3D virtual preoperative planning' group. Surgeons will plan their surgery using traditional planning tools (X-rays and CT scan) or traditional planning tools ánd the 3D virtual planning software. 6 weeks, 3 months and 6 months after surgery, participants will be asked to fill in 2 questionnaires about knee pain and knee function. After surgery a CT scan or X-ray will be performed conform standard of care in the hospital.
Detailed Description
Patients with tibial plateau fractures are traditionally challenging to treat, especially the complex fracture patterns in which anatomic reconstruction of the articular surface can be very demanding. In a previous study, the researchteam showed that surgical decision-making should be guided by recognition of specific fracture characteristics, rather than the 'classic' classification of fractures by Schatzker. Recognition of these specific tibial plateau fracture patterns has been proven reliable and reproducible to guide surgeons plan their approach, reduction techniques and fixation. Building on our improved understanding of (complex) tibial plateau fracture patterns, and how these specific fracture characteristics guide our surgical management, the next step includes meticulous pre-operative surgical planning to achieve the best functional results for our patients. A new state-of-the-art tool is currently available to aid surgeons in 3D virtual planning of approach, reduction strategy, and even application of hardware (i.e. size of plates and lengths of screws (https://sectra.com/medical/product/sectra-3d-trauma/). Recent studies on virtual surgical planning for fracture care have shown variable results. One study concluded that there was a significant reduction in duration of surgery in about 75.0% of all cases. Another study showed improvement of the outcomes of acetabular fracture surgery by reduced duration of the surgery and improved quality of the reduction. However, a third study showed that 3D virtual reality is inferior compared to 3D printed models on acetabular fractures in terms of interobserver agreement. In conclusion, the added value of virtual preoperative planning has yet to be determined. If virtual surgical planning is as promising as some of the previous results show, it could also have a significant impact on the surgical reduction in the treatment of tibial plateau fractures. This might lead to a reduction of duration of surgery, less complications and better patient related outcomes, such as postoperative pain and knee function. Therefore, the investigators would like to compare the conventional preoperative planning with the preoperative planning with use of the virtual planning software of Sectra AB for tibial plateau fractures in terms of duration of surgery, surgical complications and patient related outcomes. To see if the virtual planning software is comparable with the postoperative situation, the investigators would like to compare the preoperative virtual plan with the postoperative CT scan in terms of residual displacement and placement of the osteosynthesis material. Primary Objective: What is the added value of pre-operative virtual 3D surgical planning compared to traditional pre-surgical planning (i.e. surgeons' interpretation and written planning of standard 2D- and 3D CT-imaging) in patients with tibial plateau fractures in terms of duration of surgery? Secondary Objective(s): What is the added value of pre-operative virtual 3D surgical planning compared to traditional pre-surgical planning (i.e. surgeons' interpretation and written planning of standard 2D- and 3D CT-imaging) in patients with tibial plateau fractures in terms of postoperative complications? peroperative deviations of surgical planning? quality of post-operative reduction (i.e. reduction of step-off)? patient related outcomes (i.e. postoperative pain and knee function)? For this study, the investigators have chosen to perform a randomized controlled trial to reduce the risk of selection bias. Participants will be divided in two groups, where in the conventional group trauma surgeons will plan their surgery using X-rays, 2D and 3D CT scans. In the virtual group, surgeons will plan their surgery using the virtual 3D planning software of Sectra AB and X-rays, 2D and 3D CT scans. In both groups, surgery will be performed conform standard of care. This means that the preoperative planning is used as a guideline for the surgery and there will be deviated from the planning if deemed necessary for the surgery. Postoperative, surgeons will be asked to fill in questionnaires to determine deviations of the preoperative plan, time spent planning and satisfaction. Patients will be asked to fill in questionnaires to determine functional outcome and health related quality of life, a postoperative CT scan will be performed after surgery to determine quality of postoperative reduction, according to our standard-of-care. Quality of reduction on a CT or X-ray does not always match with patient experienced outcomes. Therefore, the investigators have chosen to not only measure quality of reduction, but also patient related outcomes, such as postoperative knee function and health related quality of life. Because of this possible mismatch, the investigators have chosen for reduction of operation time as our primary outcome. A longer operation time is associated with more postoperative surgical complications and blood loss. Furthermore, operation time is valuable and therefore expensive. A reduction in operation time would therefore not only have an effect on patient related outcomes, but also have effect on healthcare costs. This study will take place at the following three level I trauma centers: Flinders University Medical Center, Adelaide, Australia Radboud University Medical Center, Nijmegen, the Netherlands Massachusetts General Hospital, Boston, United States of America The investigators will ask patients who present themselves at the emergency department with a tibial plateau fracture that needs surgical treatment within 14 days of the injury to participate in this study. If they are willing to participate, an informed consent will be signed and furthermore, they will receive an information folder with specified information about this research study. Surgical residents and surgeons will be informed about this study through an e-mail with a short outline of the research. They will be asked to inform the researcher when there is a patient with a tibial plateau fracture who needs surgical treatment. The researcher will visit the emergency department or ward to inform the patient and sign the informed consent. A patient can give informed consent until two days before the planned surgery to ensure the trauma surgeon has enough time to plan the surgery thoroughly. When included, patients will randomly be divided into two groups through sealed opaque envelopes: Group 1: preoperative planning using the 3D virtual planning software of SECTRA Group 2: traditional preoperative planning (i.e. surgeons' interpretation and written planning of standard 2D- and 3D CT-imaging). Concealed randomization will be obtained with the randomizer.org software and stratified by centers. Per trauma center, the investigators will train three experienced trauma surgeons in using the SECTRA 3D virtual planning software. These surgeons perform the majority (i.e. 95%) of all patients admitted with tibial plateau fractures. The investigators will ask the surgeons from both the traditional and virtual planning groups to keep track of time they spent planning the surgery. After planning the surgery, the surgeons will fill in a questionnaire where they indicate their surgical plan (i.e. which screws and plates they are planning to use and which surgical approach they attend to perform) and time spent planning. After the surgery, the surgeons will fill in a questionnaire where they will indicate if they deviated from the pre-operative plan and if they are satisfied with the postoperative result. Using the operative notes, the investigators will determine the used screws, plates and surgical approach and the total duration of surgery. Postoperative patients will get a CT-scan to determine the quality of the postoperative reduction. After 6 weeks, 12 weeks and 6 months the investigators will determine functional outcome and health related quality of life using the 'Knee injury and Osteoarthritis Score' (KOOS) questionnaire, and the Short Form - 36 (SF-36) questionnaire. The investigators will use CastorEDC for creating the patient and surgeon questionnaires and for storing patient information at the secured digital research environment of Radboud University Medical Center. All patient and surgeon information will be pseudonymized by the department of Radiology and Nuclear Medicine of the participating hospital, therefore subjects privacy is protected. This key will be deleted after data collection is finished. For analysis, these questionnaires will be exported to SPSS. The data of the statistical analysis and the results will also be stored at the secured digital research environment. The data will be kept for 15 years. Only researchers involved in the study have access to the data.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional planning group
Arm Type
No Intervention
Arm Description
Conventional preoperative planning using x-rays and 2D and 3D CT scan
Arm Title
3D virtual planning group
Arm Type
Experimental
Arm Description
Preoperative planning using x-rays, 2D and 3D CT scans and 3D virtual planning software
Intervention Type
Other
Intervention Name(s)
3D virtual planning software
Intervention Description
3D virtual planning software developed by Sectra AB (Linköping, Sweden)
Primary Outcome Measure Information:
Title
Duration of surgery
Description
Time in minutes from start of surgery till end of surgery
Time Frame
Intraoperative
Secondary Outcome Measure Information:
Title
Blood loss
Description
Amount of blood loss in milliliters during surgery
Time Frame
Intraoperative
Title
Surgical complications
Description
Number of complications related to performed surgery or to condition
Time Frame
up to 30 days postoperative
Title
Perioperative deviations
Description
Number of perioperative deviations of the perioperative plan
Time Frame
Immediately after x-ray or CT scan is performed
Title
Quality of reduction
Description
Postoperative step off in millimeters as measured on postoperative CT scan or X-ray
Time Frame
Immediately after x-ray or CT scan is performed
Title
Quality of reduction
Description
Postoperative gap in millimeters as measured on postoperative CT scan or X-ray
Time Frame
Immediately after x-ray or CT scan is performed
Title
Postoperative knee function
Description
Participant indicated postoperative knee function as measured with the KOOS questionnaire (score between 0 and 100, with 100 being no pain/restrictions in knee function) and SF-36 questionnaire (score between 0 and 100, with 100 being no limitations in social functioning)
Time Frame
Measured at 6 weeks, 3 months and 6 months postoperative
Title
Postoperative knee pain
Description
Participant indicated postoperative knee function as measured with the KOOS questionnaire (score between 0 and 100, with 100 being no pain/restrictions in knee function) and SF-36 questionnaire (score between 0 and 100, with 100 being no limitations in social functioning)
Time Frame
Measured at 6 weeks, 3 months and 6 months postoperative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • Adult patients of 18 years or older with a tibial plateau fracture who will receive surgical treatment for this fracture Exclusion Criteria: patients with (general) bone diseases or osseous malformation syndromes, ipsilateral limb fractures, complicated tibial plateau fractures that need an external fixator, previous tibial plateau fractures previous surgical treatment of the tibial plateau
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jellina Huitema, MD
Phone
+31243613808
Email
jellina.huitema@radboudumc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Job Doornberg, Professor
Email
j.n.doornberg@umcg.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Job Doornberg, Professor
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jellina Huitema, MD
Email
jhuitema@mgh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Marilyn Heng, MD
Email
mheng@mgh.harvard.edu
Facility Name
Flinders Medical Center
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5042
Country
Australia
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruurd Jaarsma, Professor
Email
ruurd.jaarsma@sa.gov.au
First Name & Middle Initial & Last Name & Degree
Nynke van der Gaast, MD
Email
nynke.vandergaast@radboudumc.nl
Facility Name
Radboud University Medical Center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jellina Huitema, MD
Phone
+31243613808
Email
jellina.huitema@radboudumc.nl
First Name & Middle Initial & Last Name & Degree
Erik Hermans, PhD, MD
Phone
+31243613808
Email
erik.hermans@radboudumc.nl

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We will use the digital research environment (DRE), developed by a collaboration of hospitals in the Netherlands, to share anonymized individual participant data between the three participating centers. Participant data that will be shared is: 3D Virtual planning software Time spent planning Fracture Characteristics Surgeon satisfaction Patient Demographics Age Sex Mechanism of injury Comorbidities BMI Duration of surgery Number of complications Perioperative deviations Quality of reduction Knee pain and function Surgeon characteristics Area of practice Sex Specialization Years in practice
IPD Sharing Time Frame
Data will become available after inclusion of the first patient. The data will be vailable until 6 months after inclusion of the last patient
IPD Sharing Access Criteria
Only the research team will have access to the data
IPD Sharing URL
https://mydre.org/

Learn more about this trial

3D Virtual Planning for Tibial Plateau Fractures

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