Status:
RECRUITING
Comparison of Two Different Regional Analgesia Techniques for Patients Undergoing Total Knee Arthroplasty
Lead Sponsor:
Centre Hospitalier Universitaire Vaudois
Conditions:
Analgesia
Arthropathy of Knee
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The objective of this clinical trial is to compare two regional analgesia techniques in patients undergoing total knee arthroplasty: IPACK (Infiltration of local anesthetic between the Popliteal Arter...
Detailed Description
The aim of this randomized controlled double blinded trail is to compare an analgesic effect of an IPACK (Infiltration of local anesthetic between the Popliteal Artery and Capsule of the Knee) block v...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists classification I-III
- 18 yo or older
- patients scheduled for total knee arthroplasty under central spinal anesthesia
- informed consent signed
Exclusion
- Refusal or inability for informed consent
- Known allergies to ropivacaine, acetaminophen, ibuprofen, ketorolac, morphine, ondansetron or dexamethasone
- Secondary surgical revision
- Opioid treatment such as morphine, hydrocodone, hydromorphone, tramadol, methadone, fentanyl, buprenorphine or codeine
- Bleeding diathesis
- Neurological deficit
- Known renal insufficiency (eGFR \<45 ml/min)
- Known hepatic insufficiency (Child score B or C)
- Alcohol abuse
Key Trial Info
Start Date :
February 8 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 18 2025
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT06179641
Start Date
February 8 2024
End Date
July 18 2025
Last Update
February 9 2024
Active Locations (1)
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1
University Hospital of Lausanne
Lausanne, Canton of Vaud, Switzerland, 1011