Polyaxial Locking Plate Osteosynthesis in Proximal Tibia Fractures
Primary Purpose
Tibia Plateau Fracture
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
VA-LCP
NCB-PT
Sponsored by
About this trial
This is an interventional treatment trial for Tibia Plateau Fracture focused on measuring Proximal tibia fracture, clinical trial, polyaxial locking plate, outcome, osteosynthesis
Eligibility Criteria
Inclusion Criteria:
- patients aged 25 to 82 with a proximal tibia fractures (AO/ OTA 41 B-C) and indication for locking plate osteosynthesis
Exclusion Criteria:
- Pathological fractures
- pregnancy
- adolescence (age <18 y)
- prisoners
- patients currently put under tutelage
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
VA-LCP
NCB-PT
Arm Description
Osteosynthesis with a VA-LCP system
Osteosynthesis with a NCB-PT system
Outcomes
Primary Outcome Measures
Rasmussen score
functionality and pain
Tegner score
activity, functionality
Rasmussen score (radiological part)
articular surface depression, condylar widening and fragment angulation
Fracture healing
Categorized in accordance to the phases of bone healing: A = cloudy cortical edges and condensation (granulation phase), B = defined edges bridging, lamellar bone deposition, cartilage callus formation (reparative phase), C = remodelling to original bone contour (remodelling phase), D = non-union
Lysholm score
functionality and pain
Oxford knee score
functionality and pain
Munich knee questionnaire
pain, daily life and sports activity, functionality
Secondary Outcome Measures
Full Information
NCT ID
NCT04680247
First Posted
December 7, 2020
Last Updated
December 17, 2020
Sponsor
Technical University of Munich
1. Study Identification
Unique Protocol Identification Number
NCT04680247
Brief Title
Polyaxial Locking Plate Osteosynthesis in Proximal Tibia Fractures
Official Title
Outcome After Polyaxial Locking Plate Osteosynthesis in Proximal Tibia Fractures: a Prospective Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
October 5, 2013 (Actual)
Primary Completion Date
December 14, 2016 (Actual)
Study Completion Date
January 1, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Technical University of Munich
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
From October 2013 28 patients with proximal tibia fractures (AO/ASIF 41 B-C) were included in this study. According to our treatment algorithm for this entity Patients were assigned into two groups and treated with different polyaxial locking plates (NCB-PT®, Zimmer vs. VA-LCP® Synthes). After 12 months postoperative the investigators conducted clinical and radiological follow-ups.
Detailed Description
Prior to the onset of the study, the approval by the medical ethics committee of the Technical University of Munich (TUM) (Trial Number: 5923/13) was obtained. During a period from October 2013 to December 2015 the investigators enrolled 28 patients aged 25 to 82 into our study. All patients suffered a fracture of the proximal tibia. The fractures were classified according to the AO/OTA classification. Every one of the 28 patients had an indication for locking plate osteosynthesis. The investigators included all type 41-B fractures and all type 41-C fractures. Pathological fractures, pregnancy, adolescence (age <18 y), prisoners and patients currently put under tutelage were excluded. The patients were scheduled for a locking plate osteosynthesis with either the NCB-PT® system or the VA-LCP® system. The discission was made by using our internal treatment algorithm for proximal tibia fractures. Age, bone quality, fracture configuration, allergies and distal fracture extension were among the criteria the investigators took into account to determine the plate type.
Surgical technique
The surgical technique was standardized, as far as possible. All surgeons agreed upon the following procedure. The anterolateral approach was used in all cases. Depending on the fracture type and the damaged column the standard approach was supplemented with either a posterolateral approach or a posteromedial approach. After arthrotomy and suturing of the lateral meniscus the fracture was reduced. This was performed under direct visual control of the joint surface and/or image intensifier. K-wires and/or a reduction forceps was used to secure the reduction. Afterwards the locking plate was inserted and temporarily fixed to the bone with K-wires. After checking the correct position of the plate with an image intensifier the screws were applied. In case of VA-LCP®, additional lag screws have been inserted at discretion of the surgeon. All patients received a perioperative single shot antibiotics. Our postoperative procedure consisted of a partial weight bearing for 6 weeks for all patients. Regarding the allowed range of motion the investigators distinguished two different groups: patient who received an arthrotomy and a refixation of the meniscus ought to comply with a limited range of motion for 6 weeks overall (week 1-2 30/0/0, week 3-4 60/0/0, week 5-6 90/0/0, week 7 free RoM). Patients with no arthrotomy were allowed free range of motion immediately after surgery.
Postoperative clinical and radiologic follow-up The investigators conducted the follow up after 12 months. The clinical evaluation was performed in our trauma outpatient clinic. With the help of standardized questionnaires, the investigators examined amongst others: the range of motion, cruciate ligament/ collateral ligament instability and meniscus signs to measure the clinical outcome. Also the investigators collected data from 5 different knee scoring systems, the Tegner score, the Rasmussen score (clinical part), the Oxford knee score the Munich knee questionnaire and the Lysholm score. To measure the patient satisfaction the investigators used the SF36 (36-Item Short-Form Health Survey) Besides the clinical data the primary outcome measurements also included standardized, blinded radiological evaluation. The investigators conducted X-ray examinations in two plains (AP, lateral view) and examined them for signs of screw misplacement, primary/secondary loss of reduction, non-union and malalignment.
Statistics The statistical analysis was performed with the program GraphPad Prism 6 (GraphPad Software Inc., La Jolla, CA, USA). To check the data for standard distribution the investigators used the D'Agostino omnibus K2 test. For continuous parametric variables the investigators used the Student's t-test, for non-parametric variables the Mann-Whitney U test and for binominal variables the Fisher's exact test. In all analysis the significance level was set at a p-value <0,05, the investigators plotted the data as mean values ± SEM.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tibia Plateau Fracture
Keywords
Proximal tibia fracture, clinical trial, polyaxial locking plate, outcome, osteosynthesis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
VA-LCP
Arm Type
Active Comparator
Arm Description
Osteosynthesis with a VA-LCP system
Arm Title
NCB-PT
Arm Type
Active Comparator
Arm Description
Osteosynthesis with a NCB-PT system
Intervention Type
Procedure
Intervention Name(s)
VA-LCP
Intervention Description
Surgery using the VA-LCP implant
Intervention Type
Procedure
Intervention Name(s)
NCB-PT
Intervention Description
Surgery using the NCB-PT implant
Primary Outcome Measure Information:
Title
Rasmussen score
Description
functionality and pain
Time Frame
12 months
Title
Tegner score
Description
activity, functionality
Time Frame
12 months
Title
Rasmussen score (radiological part)
Description
articular surface depression, condylar widening and fragment angulation
Time Frame
12 months
Title
Fracture healing
Description
Categorized in accordance to the phases of bone healing: A = cloudy cortical edges and condensation (granulation phase), B = defined edges bridging, lamellar bone deposition, cartilage callus formation (reparative phase), C = remodelling to original bone contour (remodelling phase), D = non-union
Time Frame
12 months
Title
Lysholm score
Description
functionality and pain
Time Frame
12 months
Title
Oxford knee score
Description
functionality and pain
Time Frame
12 months
Title
Munich knee questionnaire
Description
pain, daily life and sports activity, functionality
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients aged 25 to 82 with a proximal tibia fractures (AO/ OTA 41 B-C) and indication for locking plate osteosynthesis
Exclusion Criteria:
Pathological fractures
pregnancy
adolescence (age <18 y)
prisoners
patients currently put under tutelage
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Biberthaler, Prof
Organizational Affiliation
Technical University of Munich Klinikum rechts der Isar, Department of Trauma Surgery
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Marc Hanschen, PD
Organizational Affiliation
Technical University of Munich Klinikum rechts der Isar, Department of Trauma Surgery
Official's Role
Study Chair
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33736638
Citation
Volk D, Neumaier M, Einhellig H, Biberthaler P, Hanschen M. Outcome after polyaxial locking plate osteosynthesis in proximal tibia fractures: a prospective clinical trial. BMC Musculoskelet Disord. 2021 Mar 18;22(1):286. doi: 10.1186/s12891-021-04158-z.
Results Reference
derived
Learn more about this trial
Polyaxial Locking Plate Osteosynthesis in Proximal Tibia Fractures
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