Multimodal DVT Protocol in Tourniquet-less Total Knee Arthroplasty
Primary Purpose
Deep Vein Thrombosis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
extended compression
Aspirin
Sponsored by
About this trial
This is an interventional prevention trial for Deep Vein Thrombosis focused on measuring DVT, Total Knee Arthroplasty
Eligibility Criteria
Inclusion Criteria:
- TKA candidacy, osteoarthritis, patients able to understand study intent, and agree to study participation
Exclusion Criteria:
- Subjects with personal or family history of DVT, currently taking antiplatelet/anticoagulant drugs, genetic risk factor positive for VTE, pronounced thrombocytopenia, GI bleed within 6 months of surgery, NSAID intolerance, orthopaedic and medical co-morbidities that would prevent postoperative rapid mobilization and compliance with MCD such as extra-articular pathology with referred pain to the knee (spinal stenosis, neuropathy, ipsilateral hip disease), severe knee deformity, post-traumatic and inflammatory arthritis, BMI above 40, active knee sepsis, remote sites of active infection, ASA class > lll, cardiac disease failing medical clearance, severe liver disease, peripheral artery disease, seizure disorder, alcohol abuse, smoking abuse
Sites / Locations
- Good Samaritan Hosptial
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Aspirin only
extended compression
Arm Description
Patients receive aspirin therapy
aspirin and extended compression therapy in combination
Outcomes
Primary Outcome Measures
DVT Occurence
DVT Occurence measured by physical assessment and duplex ultrasound images for DVT detection
Secondary Outcome Measures
Patient Satisfaction
Patient satisfaction will be measured 10 days postop using the EuroQol standardized instrument
Mobilization
Patient activity level will be measured using the standardized UCLA Activity Score
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02102828
Brief Title
Multimodal DVT Protocol in Tourniquet-less Total Knee Arthroplasty
Official Title
Efficacy of Prolonged Distal Calf Compression as Part of a Multimodal DVT Protocol in Tourniquet-less Total Knee Arthroplasty: a Randomized Clinical Trial in 100 Patients
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
TriHealth Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The Cothera VPulse(tm) mechanical compression device (MCD) combines rapid intermittent sequential compression with cold therapy and is designed for single patient use in the home. Additionally, it can track patient compliance. This study will examine if there is a difference in deep vein thrombosis (DVT) occurrence over 3 weeks after tourniquet-less total knee arthroplasty (TKA) and multimodal prophylaxis with or without extended MCD use in a cooling device/MCD system.
Detailed Description
In recent years there has been significant progress towards more effective and practical thromboprophylaxis in joint replacement surgeries. Since Aspirin 325mg twice daily has been recently included as a nationally approved venous thromboembolism (VTE) prophylaxis in the Surgical Care Improvement Project (SCIP) protocols for low risk total knee arthroplasty (TKA) patients, it is necessary to optimize multimodal prophylaxis methods. These include reduced tourniquet time, early mobilization, and mechanical compression devices (MCDs). MCDs are commonly used as part of the in-hospital VTE prophylaxis measures; however, it has not been demonstrated in clinical trials that optimal prophylaxis methods would be enhanced by prolonged use of a MCD after discharge. In order to achieve this, a potentially valuable solution has recently been made available to the outpatient population. The Cothera VPulse(tm) is a MCD that combines rapid intermittent sequential compression with cold therapy. It is designed for single patient use in the home and includes technology to track patient compliance. The purpose of this study is to examine if there is a difference in DVT occurrence over 3 weeks after tourniquet-less TKA and multimodal prophylaxis with or without extended MCD use in a cooling device/MCD system.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis
Keywords
DVT, Total Knee Arthroplasty
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Aspirin only
Arm Type
Placebo Comparator
Arm Description
Patients receive aspirin therapy
Arm Title
extended compression
Arm Type
Experimental
Arm Description
aspirin and extended compression therapy in combination
Intervention Type
Device
Intervention Name(s)
extended compression
Intervention Description
Home use of extended compression therapy and aspirin
Intervention Type
Other
Intervention Name(s)
Aspirin
Intervention Description
standard therapy of aspirin
Primary Outcome Measure Information:
Title
DVT Occurence
Description
DVT Occurence measured by physical assessment and duplex ultrasound images for DVT detection
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Patient Satisfaction
Description
Patient satisfaction will be measured 10 days postop using the EuroQol standardized instrument
Time Frame
10 days
Title
Mobilization
Description
Patient activity level will be measured using the standardized UCLA Activity Score
Time Frame
10 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
TKA candidacy, osteoarthritis, patients able to understand study intent, and agree to study participation
Exclusion Criteria:
Subjects with personal or family history of DVT, currently taking antiplatelet/anticoagulant drugs, genetic risk factor positive for VTE, pronounced thrombocytopenia, GI bleed within 6 months of surgery, NSAID intolerance, orthopaedic and medical co-morbidities that would prevent postoperative rapid mobilization and compliance with MCD such as extra-articular pathology with referred pain to the knee (spinal stenosis, neuropathy, ipsilateral hip disease), severe knee deformity, post-traumatic and inflammatory arthritis, BMI above 40, active knee sepsis, remote sites of active infection, ASA class > lll, cardiac disease failing medical clearance, severe liver disease, peripheral artery disease, seizure disorder, alcohol abuse, smoking abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark A Snyder, MD
Organizational Affiliation
TriHealth Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Good Samaritan Hosptial
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45220
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
28159420
Citation
Snyder MA, Sympson AN, Scheuerman CM, Gregg JL, Hussain LR. Efficacy in Deep Vein Thrombosis Prevention With Extended Mechanical Compression Device Therapy and Prophylactic Aspirin Following Total Knee Arthroplasty: A Randomized Control Trial. J Arthroplasty. 2017 May;32(5):1478-1482. doi: 10.1016/j.arth.2016.12.027. Epub 2016 Dec 23.
Results Reference
derived
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Multimodal DVT Protocol in Tourniquet-less Total Knee Arthroplasty
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