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Clinical Trial Summary

To prove that total knee arthroplasty can be performed with little, if any need for opioids by using a combination of patient education, optimized pre-op and post-op pain and recovery protocols. The goal being opioid-free total knee arthroplasty.


Clinical Trial Description

All study patients will receive a standardized protocol

- All surgical procedures performed by single surgeon using same implants, approach, pre-op and post-op optimization, and simplified pain protocol at a single hospital or surgery center

- Will attempt to minimize the number of anesthesiologists to further control variability in care

Methods:

1. Pre-op Optimization

- All patients enroll in education program

- All patients have optimized BMI, hemoglobin, albumin, glucose control-A1C, and blood pressure

2. Total Joint Procedure

- Tourniquet-free cemented total knee arthroplasty is performed with intra-articular block

3. Data Collection

- Electronic medical record chart review

- Pre-op assessment and Post-op assessment (post anesthesia care unit (PACU), Phase II-prior to discharge

- Phone calls after discharge

- Follow-up assessment in surgeon's office

- Swift path / KOOS JR surveys

4. Pain Management Regimen

- pre-op physical therapy teaching

- post-op multimodal pain regimen ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03647709
Study type Observational
Source St. Elizabeth Medical Center, Utica, NY
Contact
Status Completed
Phase
Start date October 1, 2018
Completion date April 30, 2020

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