Total Knee Arthroplasty - Accelerated Recovery Without Tourniquet
Primary Purpose
Arthropathy of Knee Joint
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Total Knee Arthroplasty
Sponsored by
About this trial
This is an interventional treatment trial for Arthropathy of Knee Joint focused on measuring Prothesis fixation, Bloodlessness
Eligibility Criteria
Inclusion Criteria:
- Patients with symptomatic and radiographic verified knee symptoms, selected for primary unilateral total knee joint replacement (TKR)
- Age 50 and above (not older than 85)
- BMI < 35 and height >160 cm
- No severe cardiovascular conditions
- No previously knee surgery done in the same knee
- Oral and written acceptance
Exclusion Criteria:
- Severe obesity
- rheumatic diseases
- Absence of pulse in foot
- Diabetes
- Previous operation in concerning knee
- Lack of informed consent or ability to read / understand Danish
Sites / Locations
- Aalborg University Hospital, Northern Orthopaedic Division, Department of Arthroplasty, Farsoe Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
With Tourniquet
Without Tourniquet
Arm Description
Total Knee Arthroplasty. Surgery performed during use of a tourniquet.
Total Knee Arthroplasty. Surgery performed without use of a tourniquet.
Outcomes
Primary Outcome Measures
Determine whether prosthesis fixation, measured by RSA, is affected by tourniquet use.
To determine whether prosthesis fixation, measured by RSA, is affected by tourniquet use. Because third generation cements secure prosthesis fixation, we do not expect to find any clinically significant migration (less than 2 mm) 2 years after surgery.
Secondary Outcome Measures
To investigate the advantages and disadvantages of tourniquet use, including whether not using a tourniquet reduces pain, facilitates mobilisation and recovery, and shortens length of stay.
Full Information
NCT ID
NCT01309035
First Posted
January 14, 2011
Last Updated
January 29, 2015
Sponsor
Northern Orthopaedic Division, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT01309035
Brief Title
Total Knee Arthroplasty - Accelerated Recovery Without Tourniquet
Official Title
Total Knee Arthroplasty - Accelerated Recovery Without Tourniquet
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Northern Orthopaedic Division, Denmark
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Introduction:
Approximately 7000 total knee replacements (TKAs) are done every year. More than 90% of these knee replacements are performed with the use of bone cement. Traditionally, a tourniquet has been, used to reduce the bleeding during surgery, enabling surgeons to perform delicate dissections in a bloodless operative field.
A tourniquet can be defined as a constricting or compressing device used to control temporarily venous and arterial circulation to an extremity. Pressure is applied circumferentially on the skin and underlying tissues of a limb. This pressure is transferred to the walls of vessels, causing them to become occluded.
It is well known that applying a tourniquet for more than 1 to 2 hours is associated with a number of disadvantages, for instance, severe pain and muscle effects during the first postoperative day, thereby slowing rehabilitation.
Other side effects related to tourniquet use, include pulmonary embolus caused by venous thrombosis and arterial thrombosis as a result of the dislodgement of an arterial plaque. Furthermore, tourniquet-induced hypertension with general anaesthesia, muscle injury, a wide spectrum of neurologic injuries, and tissue changes (Oedema compartment syndrome, post-tourniquet syndrome) have been reported. An important fact is that bleeding affects the quality of binding between bone and cement and thereby fixation of the knee prosthesis? Since the introduction of modern cementing techniques, no previous clinical studies have investigated the advantages or disadvantages of tourniquet use in knee replacement surgery.
Aims/hypothesis of the study:
To investigate the advantages and disadvantages of tourniquet use, including whether not using a tourniquet reduces pain, facilitates mobilisation and recovery, and shortens length of stay.
To study whether use of a tourniquet affects leg muscles during and after surgery, as measured by with use of microdialysis to quantify level of ischemia .
To determine whether prosthesis fixation, measured by RSA, is affected by tourniquet use. Because third generation cements secure prosthesis fixation, the investigators do not expect to find any clinically significant migration (less than 2 mm) 2 years after surgery.
Perspectives:
The investigators hope that the results of our study will improve rehabilitation regimes so that patients will experience less pain after surgery and thus achieve more rapid mobilisation and return to their daily lives.
Detailed Description
Design
Patients being able to participate in this study all have to fulfill the given inclusion criteria:
Patients with symptomatic and radiographic verified knee symptoms, selected for primary unilateral total knee joint replacement (TKA)
Age 50 and above (not older than 85)
BMI < 35 and height >160 cm
No severe cardiovascular conditions
No previously knee surgery done in the same knee
Oral and written acceptance
A group concerning 2 x 30 patients will be randomized into two groups. Either an intervention group, with absence of tourniquet or a control group with tourniquet. Which group they will belong to, is blinded to patient and surgeon until they reach operation room. The operation will be performed as usual, but with exception of two additional procedures. During operation small spheric tantalum pellets are placed around the prosthesis. Furthermore patients are prepared for microdialysis, which contain placement of 3 catheters: one in each thigh and one subcutaneously in the abdomen.
Microdialysis is a unique technique to monitor the chemistry of the extracellular space in living tissue. It is primarily used for In Vivo determinations of endogenous metabolites, thus serving as an indicator for ischemia.
RSA is precision radiology where the small pellets are visual on x-ray. Using computer a 3D image is created and the pellets serve as markers. These markers will be measured every 6 months showing whether a possible migration of the prosthesis is occurring and thereby indicating a loosening.
Out-patient treatment Patients will among other things be followed by clinical functional scores, registration of analgetica use, conventional X-ray and RSA In the long run the perspective is that surgery concerning knee replacements will be conducted without the use of tourniquet and thereby reducing the pain of the patients without compromising the end result of the operation, namely the fixation of the prosthesis.
Permissions approved by the Regional Committee on Biomedical Research Ethics, Region of Northern Jutland and Danish Data Protection Agency.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthropathy of Knee Joint
Keywords
Prothesis fixation, Bloodlessness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Actual)
8. Arms, Groups, and Interventions
Arm Title
With Tourniquet
Arm Type
Active Comparator
Arm Description
Total Knee Arthroplasty. Surgery performed during use of a tourniquet.
Arm Title
Without Tourniquet
Arm Type
Experimental
Arm Description
Total Knee Arthroplasty. Surgery performed without use of a tourniquet.
Intervention Type
Procedure
Intervention Name(s)
Total Knee Arthroplasty
Intervention Description
Surgery for OA knee pains
Primary Outcome Measure Information:
Title
Determine whether prosthesis fixation, measured by RSA, is affected by tourniquet use.
Description
To determine whether prosthesis fixation, measured by RSA, is affected by tourniquet use. Because third generation cements secure prosthesis fixation, we do not expect to find any clinically significant migration (less than 2 mm) 2 years after surgery.
Time Frame
1.Feb 2011 -1 jan 2013
Secondary Outcome Measure Information:
Title
To investigate the advantages and disadvantages of tourniquet use, including whether not using a tourniquet reduces pain, facilitates mobilisation and recovery, and shortens length of stay.
Time Frame
1.feb 2011 - 1.jan 2013
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with symptomatic and radiographic verified knee symptoms, selected for primary unilateral total knee joint replacement (TKR)
Age 50 and above (not older than 85)
BMI < 35 and height >160 cm
No severe cardiovascular conditions
No previously knee surgery done in the same knee
Oral and written acceptance
Exclusion Criteria:
Severe obesity
rheumatic diseases
Absence of pulse in foot
Diabetes
Previous operation in concerning knee
Lack of informed consent or ability to read / understand Danish
Facility Information:
Facility Name
Aalborg University Hospital, Northern Orthopaedic Division, Department of Arthroplasty, Farsoe Clinic
City
Farsoe
State/Province
Northern Jutland
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Total Knee Arthroplasty - Accelerated Recovery Without Tourniquet
We'll reach out to this number within 24 hrs