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Comparison of Pinless Navigation and Conventional Method in Total Knee Arthroplasty

Primary Purpose

Osteoarthritis, Knee

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Primary total knee replacement by pinless navigation (Orthomap Express,Stryker, Michigan)
Primary total knee replacement by traditional jig and minimally invasive technique
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Total knee arthroplasty, pinless, navigation, alignment, minimal invasive

Eligibility Criteria

50 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with osteoarthritis of the knee secondary to degeneration, inflammatory arthritis, gouty arthritis, posttraumatic arthritis, and undergoing primary unilateral minimally invasive TKA
  2. Age > 50 years and < 90 years
  3. Failure of medical treatment or rehabilitation.
  4. Hemoglobin > 11g/dl,
  5. No use of non-steroid anti-inflammatory agent one week before operation

Exclusion Criteria:

  1. Preoperative Hemoglobin <11 g/dl
  2. History of infection or intraarticular fracture of the affective knee
  3. Renal function deficiency (GFR <30 ml/min/1.73m2)
  4. Elevated liver enzyme (AST/ALT level are more than twice normal range) , history of liver cirrhosis, impaired liver function(elevated total bilirubin level) and coagulopathy (including long-term use anticoagulant)
  5. History of deep vein thrombosis, ischemic heart disease, cardiac arrythmia requiring life-long anti-coagulants, or stroke
  6. Contraindications of tranexamic acid, rivaroxaban, or the excipients
  7. Allergy to tranexamic acid, rivaroxaban, or the excipients
  8. Coagulopathy or bleeding tendency caused by organ dysfunction, such as cirrhosis, bone marrow suppression etc.
  9. Patient who have active bleeding disorder, such as intracranial hemorrhage, upper GI bleeding, hematuria

Sites / Locations

  • Kaohsiung Chang Gung Memorial HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Group I

Group II

Arm Description

Primary total knee replacement by pinless navigation and minimally invasive technique

Primary total knee replacement by traditional jig and minimally invasive technique

Outcomes

Primary Outcome Measures

Radiographic outcome: the mechanical alignment (MA)
The mechanical alignment (MA): an angle between the mechanical axis of the femur and the tibial shaft axis
Radiographic outcome: anatomic alignment (AA)
The anatomic alignment (AA): an angle between the axis of the femoral shaft and the tibial shaft axis
Radiographic outcome: femoral bowing angle (FBA)
The femoral bowing angle (FBA): the angle between the distal and proximal femoral anatomical axes
Radiographic outcome: coronal femoral-component angle (CFA)
Tthe angle between the femoral mechanical axis and the femoral component
Radiographic outcome: coronal tibia-component angle (CTA)
The angle between the tibial shaft axis and the tibial component

Secondary Outcome Measures

Total Blood Loss
The total blood loss was calculated according to Nadler et al., which uses maximum postoperative decrease of the Hb level adjusted for weight and height of the patient. Total blood loss consists of amount of blood loss calculated from the maximum Hb loss and amount of blood transfused
Blood transfusion rate
Record the event of blood transfusion, and calculate the incidence of transfusion
Operating Time
Time needed for the surgical procedure (skin to skin) is recorded
Surgical wound length
The surgical wound length at full extension of knee is also recorded
Wound complications
Any wound complications including superficial infection, wound dehiscence, poor healing, etc. are all recorded
Venous thromboembolism
perform duplex ultrasound study of both lower limbs in all patients on postoperative day 4

Full Information

First Posted
January 17, 2020
Last Updated
January 29, 2020
Sponsor
Chang Gung Memorial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04235283
Brief Title
Comparison of Pinless Navigation and Conventional Method in Total Knee Arthroplasty
Official Title
Comparison of the Radiographic Outcomes and Total Blood Loss Between Pinless Navigation and Conventional Method in Minimally Invasive Total Knee Arthroplasty
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to conduct a prospective randomized clinical trial to compare the accuracy of prosthesis, radiographic alignment, total blood loss, the risk of venous thromboembolism between pinless-navigated total knee arthroplasty (TKA) and traditional TKA.
Detailed Description
Minimal invasive surgery total knee arthroplasty (MIS-TKA) is an excellent surgical procedure for patients with end-stage knee diseases and can reduce the postoperative complications compared with traditional TKA procedures. However, MIS-TKA procedures require a long learning curve to avoid malposition of prosthesis. In previous studies have demonstrated that the position of prosthesis and the postoperative mechanical axis are critical factors of outcome. Malposition of prosthesis and deviation more than 3 degrees of mechanical axis will lead to asymmetrical tibia-femoral tracking between prosthesis with the wear of linear, and increase the incidence of prosthesis loosening. Computer navigation assisted system has been used in TKA procedures for more than one decade and has been proven to improve the accuracy of prosthesis placement and postoperative mechanical alignment. Moreover, navigated TKA avoids the use of intramedullary guide and preserve the medullary cavity of femur, so the risks of bleeding and venous thromboembolism are reduced. However, traditional navigation system requires additional procedure to set reference arrays with pin fixation of femur and tibia. Pin wound complications including bleeding, infection, and iatrogenic fracture were reported. Moreover, traditional navigation system requires conventional TKA approach in which the wound length of the knee will be as long as 15 to 20 cm. Therefore a combination of new navigation system with a MIS technique to perform TKA procedure is required The new pinless navigated system for TKA procedures has been developed, as the navigation tools were fixed in the surgical field without additional pin wounds. This advantage meets the rationale of MIS-TKA to take care of both minimal invasive procedures and accuracy of prosthesis placement. Therefore, the investigators want to investigate the application of this pinless navigation system in MIS-TKA procedures. Our purpose is to conduct a prospective randomized clinical trial to compare the accuracy of prosthesis, radiographic alignment, total blood loss, the risk of venous thromboembolism between pinless-navigated MIS-TKA and traditional MIS-TKA. Material and Methods: The investigators plan to enroll 100 patients who plan to undergo unilateral primary MIS-TKA and will be randomly assigned into two groups. The first group (50 patients) will be treated by pinless-navigation (Stryker, OrthoMap Express Knee Navigation) MIS-TKA, and the second group (50 patients) will undergo traditional MIS-TKA. The investigators will record the surgical wound length, surgical time cost and calculate daily hemoglobin drainage and total blood loss after TKA procedures for all patients. At 3 months after operation, the whole leg scanography, AP and lat view of knee radiography will be take and the mechanical alignment (MA), anatomic alignment (AA), femoral bowing angle (FBA), and coronal femoral-component angle (CFA), coronal tibia-component angle (CTA) in coronary view and sagittal femoral component angle (SFA), sagittal tibial component angle (STA) in lateral view will be measured. The operating time and surgical wound length in knee full extension will be recorded. All complications including bleedings, wound complications, venous thromboembolism will be recorded. Study year: one year Expecting Result The investigators anticipate that the position of prosthesis in pinless-navigated MIS-TKA is more accurate or equal to traditional MIS-TKA group. And the total blood loss in pinless-navigated MIS-TKA is less than traditional MIS-TKA group. The complication rate is similar between the two groups

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Total knee arthroplasty, pinless, navigation, alignment, minimal invasive

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Enroll 100 patients who plan to undergo unilateral primary MIS-TKA and will be randomly assigned into two groups. The first group (50 patients) will be treated by pinless-navigation (Stryker, OrthoMap Express Knee Navigation) MIS-TKA, and the second group (50 patients) will undergo traditional MIS-TKA.
Masking
ParticipantOutcomes Assessor
Masking Description
This study proposed 1:1 randomization into pinless navigation and conventional technique. Each patient who enrolled in this study will be given sequence study number, and the chief surgeon will draw lots to decide which group will be assigned in. The patient and the independent reviewer are kept blinded
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group I
Arm Type
Experimental
Arm Description
Primary total knee replacement by pinless navigation and minimally invasive technique
Arm Title
Group II
Arm Type
Active Comparator
Arm Description
Primary total knee replacement by traditional jig and minimally invasive technique
Intervention Type
Device
Intervention Name(s)
Primary total knee replacement by pinless navigation (Orthomap Express,Stryker, Michigan)
Intervention Description
The varus/valgus, extension/flexion, thickness of distal cut of femur was determined and done by pinless navigation system. After cutting, the instant information of resection level can show on the display screen. If the alignment is satisfying, the anterior/posterior femoral cut, chamfer cut and box resection were done by conventional jig
Intervention Type
Procedure
Intervention Name(s)
Primary total knee replacement by traditional jig and minimally invasive technique
Intervention Description
The femoral alignment was determined by intramedullary guide. The femoral alignment jig was set to 5-7 degree valgus dependent on the preoperative radiograph. A bone plug is impacted into the entry hole of femoral medullary canal before prosthesis placement.
Primary Outcome Measure Information:
Title
Radiographic outcome: the mechanical alignment (MA)
Description
The mechanical alignment (MA): an angle between the mechanical axis of the femur and the tibial shaft axis
Time Frame
Three months after operation
Title
Radiographic outcome: anatomic alignment (AA)
Description
The anatomic alignment (AA): an angle between the axis of the femoral shaft and the tibial shaft axis
Time Frame
Three months after operation
Title
Radiographic outcome: femoral bowing angle (FBA)
Description
The femoral bowing angle (FBA): the angle between the distal and proximal femoral anatomical axes
Time Frame
Three months after operation
Title
Radiographic outcome: coronal femoral-component angle (CFA)
Description
Tthe angle between the femoral mechanical axis and the femoral component
Time Frame
Three months after operation
Title
Radiographic outcome: coronal tibia-component angle (CTA)
Description
The angle between the tibial shaft axis and the tibial component
Time Frame
Three months after operation
Secondary Outcome Measure Information:
Title
Total Blood Loss
Description
The total blood loss was calculated according to Nadler et al., which uses maximum postoperative decrease of the Hb level adjusted for weight and height of the patient. Total blood loss consists of amount of blood loss calculated from the maximum Hb loss and amount of blood transfused
Time Frame
Postoperative Day 3
Title
Blood transfusion rate
Description
Record the event of blood transfusion, and calculate the incidence of transfusion
Time Frame
Three months after operation
Title
Operating Time
Description
Time needed for the surgical procedure (skin to skin) is recorded
Time Frame
After the procedure is done
Title
Surgical wound length
Description
The surgical wound length at full extension of knee is also recorded
Time Frame
After the procedure is done
Title
Wound complications
Description
Any wound complications including superficial infection, wound dehiscence, poor healing, etc. are all recorded
Time Frame
Three months after operation
Title
Venous thromboembolism
Description
perform duplex ultrasound study of both lower limbs in all patients on postoperative day 4
Time Frame
Postoperative Day 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with osteoarthritis of the knee secondary to degeneration, inflammatory arthritis, gouty arthritis, posttraumatic arthritis, and undergoing primary unilateral minimally invasive TKA Age > 50 years and < 90 years Failure of medical treatment or rehabilitation. Hemoglobin > 11g/dl, No use of non-steroid anti-inflammatory agent one week before operation Exclusion Criteria: Preoperative Hemoglobin <11 g/dl History of infection or intraarticular fracture of the affective knee Renal function deficiency (GFR <30 ml/min/1.73m2) Elevated liver enzyme (AST/ALT level are more than twice normal range) , history of liver cirrhosis, impaired liver function(elevated total bilirubin level) and coagulopathy (including long-term use anticoagulant) History of deep vein thrombosis, ischemic heart disease, cardiac arrythmia requiring life-long anti-coagulants, or stroke Contraindications of tranexamic acid, rivaroxaban, or the excipients Allergy to tranexamic acid, rivaroxaban, or the excipients Coagulopathy or bleeding tendency caused by organ dysfunction, such as cirrhosis, bone marrow suppression etc. Patient who have active bleeding disorder, such as intracranial hemorrhage, upper GI bleeding, hematuria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shih-Hsiang Yen, MD
Phone
886-7-7317123
Ext
8003
Email
yswings@cgmh.org.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jun-Wen Wang, MD
Organizational Affiliation
Department of Orthopaedic Surgery, Kaohsiung Chang Gung Memorial Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Kaohsiung Chang Gung Memorial Hospital
City
Kaohsiung
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jun-Wen Wang, MD
Phone
886-7-7317123
Email
wangjw@adm.cgmh.org.tw

12. IPD Sharing Statement

Plan to Share IPD
No
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Comparison of Pinless Navigation and Conventional Method in Total Knee Arthroplasty

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