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3D Planned Surgery of Acute Fractures Performed With 3D Guides Printed at the Point of Care (3DFRG)

Primary Purpose

Fracture Tibia, Fracture Femur, Fracture, Comminuted

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Fracture reposition with 3D printed patient specific repositions guides
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fracture Tibia focused on measuring Femur, Tibia, Comminuted fracture, 3D printing, personalized medicine

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria: Age between 18 and 99 years Comminuted shaft fracture of tibia or femur Intact contralateral tibia or femur Patient willing to participate and sign the informed consent Clear indication of surgical treatment Exclusion criteria: Refusal to sign the informed consent Abnormal contralateral bony anatomy (previous surgeries, poliomyelitis, previous injury, implants) Pregnancy Acute tumor or previous tumor disease Acute infection

Sites / Locations

  • Universitätsklinik für Orthopädische Chirurgie und TraumatologieRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

3D fracture reposition guide group

Arm Description

Comminuted tibial- or/and femur shaft fractures will be treated using 3D printed patient-specific repositions guides.

Outcomes

Primary Outcome Measures

Rotational deviation (Axial plane deviation) in degree
Planned rotational alignment versus postoperative rotational alignment.

Secondary Outcome Measures

Length deviation in mm
Planed length versus postoperative length
Frontal plane deviation in degree
Planned varus/valgus alignment versus postoperative varus/valgus alignment
Sagittal plane deviation in degree
Planned flexion/extension of the proximal and distal fracture fragments compared to the postoperative position.

Full Information

First Posted
February 13, 2023
Last Updated
March 20, 2023
Sponsor
Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT05741892
Brief Title
3D Planned Surgery of Acute Fractures Performed With 3D Guides Printed at the Point of Care
Acronym
3DFRG
Official Title
3D Planned Surgery of Acute Fractures Performed With 3D Guides Printed at the Point of Care - a Prospective Case Series
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2023 (Anticipated)
Primary Completion Date
December 1, 2024 (Anticipated)
Study Completion Date
March 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern

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
The aim of the study is to assess the accuracy of fracture reduction performed with surgical guides designed and 3D printed at the point of care in comminuted fractures of femur- and tibia-shaft.
Detailed Description
The 3D planning of surgeries and their execution with 3D printed templates adapted to the individual patient is an established procedure for elective surgeries such as corrective osteotomies for mal-united fractures. Currently, the planning and production of 3D templates are performed mainly by external companies. The duration until delivery usually exceeds four weeks. Therefore, it is not possible to use them in acute cases (e.g. acute fractures) that need to be treated surgically within a few days. The most frequent postoperative deformity in long bone shaft fractures is malrotation. In femoral fractures, clinically relevant rotational errors (>15°) occur in up to 40% of cases after surgical treatment, which either results in a poor clinical outcome or requires revision surgery. In tibial diaphyseal fractures, up to 50% of rotational errors have been reported. The higher the degree of comminution the higher the chances of malrotation postoperatively. Due to the comminuted situation, no reliable bony references exist intraoperatively and the surgeon can only estimate the correct length, axis and, rotation based on the contralateral leg. This ultimately leads to a high number of revision surgeries or poor outcomes. Porcine and human cadaveric feasibility studies conducted by the study team utilizing site 3D planned and printed reduction guides showed excellent accuracy of fracture reduction. This project aims to apply this technique to the clinical setting by conducting a clinical study. The accuracy of 3D planned surgery performed with surgical guides designed and printed at the point of care will be assessed and the complication rate will be compared to the known literature. It was hypothesized that the mean deviation between the measured postoperative rotational alignment and planned rotation alignment in patients treated for comminuted fractures of femur- and tibia-shaft treated using 3D printed reposition guides will be less than 5°. Additionally, it was hypothesized that the rate of clinically relevant deviations between postoperative rotational alignment (e.g. 15°) and planned rotation in patients treated for comminuted fractures of femur- and tibia-shaft treated using 3D printed reposition guides will be less than 10%.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fracture Tibia, Fracture Femur, Fracture, Comminuted
Keywords
Femur, Tibia, Comminuted fracture, 3D printing, personalized medicine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective case series
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
3D fracture reposition guide group
Arm Type
Experimental
Arm Description
Comminuted tibial- or/and femur shaft fractures will be treated using 3D printed patient-specific repositions guides.
Intervention Type
Device
Intervention Name(s)
Fracture reposition with 3D printed patient specific repositions guides
Intervention Description
Comminuted tibial- or/and femur shaft fractures will be treated using 3D printed patient-specific repositions guides.
Primary Outcome Measure Information:
Title
Rotational deviation (Axial plane deviation) in degree
Description
Planned rotational alignment versus postoperative rotational alignment.
Time Frame
Between 1 to 7 days postoperative, depending on the patients status
Secondary Outcome Measure Information:
Title
Length deviation in mm
Description
Planed length versus postoperative length
Time Frame
Between 1 to 7 days postoperative, depending on the patients status
Title
Frontal plane deviation in degree
Description
Planned varus/valgus alignment versus postoperative varus/valgus alignment
Time Frame
Between 1 to 7 days postoperative, depending on the patients status
Title
Sagittal plane deviation in degree
Description
Planned flexion/extension of the proximal and distal fracture fragments compared to the postoperative position.
Time Frame
Between 1 to 7 days postoperative, depending on the patients status

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Age between 18 and 99 years Comminuted shaft fracture of tibia or femur Intact contralateral tibia or femur Patient willing to participate and sign the informed consent Clear indication of surgical treatment Exclusion criteria: Refusal to sign the informed consent Abnormal contralateral bony anatomy (previous surgeries, poliomyelitis, previous injury, implants) Pregnancy Acute tumor or previous tumor disease Acute infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hecker Andreas, MD
Phone
031 632 21 11
Ext
0041
Email
andreas.hecker@insel.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Hess Silvan, MD
Phone
031 632 21 11
Ext
0041
Email
silvan.hess@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hecker Andreas, MD
Organizational Affiliation
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreas Hecker, MD
Phone
031 632 21 11
Ext
0041
Email
andreas.hecker@insel.ch
First Name & Middle Initial & Last Name & Degree
Silvan Hess, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

3D Planned Surgery of Acute Fractures Performed With 3D Guides Printed at the Point of Care

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