Total Knee Prosthesis With Continuous Block of Adductor Canal and Outcome
NCT02082067 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL
Last updated 2016-08-09
Summary
Aim of this study is to evaluate the effects of the adductor canal block on the early and medium term ( 1 month) rehabilitation compared to the continuous femoral block commonly used in the knee prosthesis.
Conditions
- Total Knee Arthroplasty
Interventions
- PROCEDURE
-
Adductor canal
Perinervous catheter (stimulong sono- Pajunk, Germany) will be insert in adductor canal through tuohy needle (18G, 100mm length) under ultrasound guidance.
- PROCEDURE
-
Femoral
Perinervous catheter (stimulong sono- Pajunk, Germany) will be insert between femoral nerve and femoral artery through tuohy needle (18G, 100mm length) under ultrasound guidance.
- PROCEDURE
-
Spinal Anesthesia
Spinal anesthesia will be perform at L3-L4 or L4-L5 level. Levobupivacaine 0,5% 12mg will be injected.
- PROCEDURE
-
Local anesthetic infusion
Continuous infusion of levobupivacaine 0,125% at 8ml/h rate through perinervous catheter until 5th postoperative day.
- PROCEDURE
-
Intravenous analgesia
Ketorolac 30mg 3 times/day and morphine Patients Control Analgesia (1mg/h, max 4mg/h) administered.
- DRUG
-
Ropivacaine 0,75%
- DRUG
-
Levobupivacaine 0,5%
- DRUG
-
Levobupivacaine 0,125%
- DRUG
-
Ketorolac 30mg
- DRUG
-
Morphine
- DEVICE
-
stimulong sono, Pajunk, Germany
Sponsors & Collaborators
-
ASST Gaetano Pini-CTO
lead OTHER
Principal Investigators
-
Gianluca Cappelleri, M.D. · ASST Gaetano Pini-CTO
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-03-31
- Primary Completion
- 2015-09-30
- Completion
- 2016-03-31
Countries
- Italy
Study Locations
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