Knee Arthroplasty Clinical Trial
Official title:
The Secret Recipe for Femoral Nerve Blockade After Total Knee Arthroplasty: A Randomized, Placebo-controlled, Double-blind Trial
Patients undergoing total knee arthroscopy (knee replacement) surgery usually receive a
femoral nerve block as part of their anesthetic care. Some centers administer the block with
a single shot of local anesthetic, which wears off several hours after surgery. Other
centers administer the block with a single shot followed by continuous infusion of local
anesthetic, typically for 2 to 5 days after surgery. The latter method, though good for pain
control, may result in decreased mobility (while the anesthetic is still active), longer
hospital stays, and greater risk of falls.
This study will see if using a lower concentration of local anesthetic for the continuous
femoral nerve block or only the initial single-shot dose will result in increased mobility
and shorter hospital stays.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05279092 -
Yale Steroid Enhanced Versus Exparel Nerveblock TKA RCT Study
|
Phase 2 | |
Completed |
NCT02581683 -
Magnesium Sulfate in Adductor Canal Blocks
|
Phase 4 | |
Completed |
NCT02413996 -
Effects of Virtual Reality Rehabilitation in Patients With Total Knee Arthroplasty
|
N/A | |
Completed |
NCT01191593 -
The Efficacy of Adductor-Canal-Blockade on Pain and Morphine Consumption After Revision Knee Arthroplasty
|
Phase 4 | |
Completed |
NCT01140815 -
Functional Performance of the Journey Deuce Bicompartmental Versus the Genesis II Total Knee System
|
Phase 4 | |
Completed |
NCT03847324 -
Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty
|
N/A | |
Active, not recruiting |
NCT06096727 -
The Energize! Study for Adults With Knee Replacement
|
N/A | |
Active, not recruiting |
NCT01705886 -
Clinical and Economic Comparison of Robot Assisted Versus Manual Knee Replacement
|
||
Terminated |
NCT01705366 -
Clinical Outcomes of Knee Replacement
|
||
Recruiting |
NCT01225484 -
Perioperative Analgesia After Knee Arthroplasty
|
Phase 4 | |
Completed |
NCT00367289 -
CT for Diagnosis of Implant Stability in Revision Arthroplasty
|
N/A | |
Withdrawn |
NCT03421938 -
Effect of Downhill-uphill Walking Exercises on Functional Level and Muscle Strength in Patients With Knee Arthroplasty.
|
N/A | |
Completed |
NCT04467970 -
Unicompartmental Knee Arthroplasty vs High Tibial Osteotomy.
|
N/A | |
Not yet recruiting |
NCT06130813 -
Increased Perioperative Communication Program in Knee Arthroplasty
|
N/A | |
Recruiting |
NCT06293144 -
the 95% Effective Dose of Ciprofol for Adjunctive Sedation Undergoing Knee Arthroplasty in Elderly People
|
Early Phase 1 | |
Active, not recruiting |
NCT04679857 -
Substitution of the PCL in TKA With UC or PS Design
|
N/A | |
Completed |
NCT06293131 -
Median Effective Dose of Ciprofol-Assisted Sedation for Elderly Patients Undergoing Knee Arthroplasty
|
Early Phase 1 | |
Completed |
NCT05091918 -
Limited Market Release - MotionSense Clinical Use Evaluation
|
N/A | |
Recruiting |
NCT02934802 -
Non-Interventional Consecutive and Prospective Study of e.Motion® PS Pro Prosthesis in the Total Knee Artroplasty
|
||
Active, not recruiting |
NCT02791477 -
Functional Results With Attune Fixed Bearing Posterior Stabilized Knee Arthroplasty (A-16)
|
N/A |