Postoperative Pain Control After Periarticular Injection During Total Knee Arthroplasty
Last updated on July 2021Recruitment
- Recruitment Status
- Enrolling by invitation
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Osteoarthritis (Knee)
- Type
- Interventional
- Phase
- Phase 4
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
Data Collection: Data will be collected from the patient's medical record after discharge Variables include: Age Sex BMI UPAT score (Universal Pain Assessment Tool)- this is assessed hourly postoperatively by nursing staff on Orthopedics Unit Patient's assessment of acceptability of pain UPAT score ...
Data Collection: Data will be collected from the patient's medical record after discharge Variables include: Age Sex BMI UPAT score (Universal Pain Assessment Tool)- this is assessed hourly postoperatively by nursing staff on Orthopedics Unit Patient's assessment of acceptability of pain UPAT score as assessed by physical therapy pre and post therapy sessions Duramorph dose Time patient arrived on the Orthopedic Unit Length of ambulation during physical therapy sessions Amount of supplementary opioids (measured in morphine equivalents) Use of anti-emetics Any complications of surgery including venous thromboembolic event, cardiac event, bleeding event Length of hospital stay The pharmacist will randomize patients to either study arm, prepare the injection and maintain dispensing records.
Tracking Information
- NCT #
- NCT02570503
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Gregory Golladay, MD Virginia Commonwealth University
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