Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02082067

Total Knee Prosthesis With Continuous Block of Adductor Canal and Outcome

Total Knee Arthroplasty & Outcome: A Prospective Randomized Comparison Between Adductor Canal Block and Femoral Nerve Block

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
ASST Gaetano Pini-CTO · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

Interventions

TypeNameDescription
PROCEDUREAdductor canalPerinervous catheter (stimulong sono- Pajunk, Germany) will be insert in adductor canal through tuohy needle (18G, 100mm length) under ultrasound guidance.
PROCEDUREFemoralPerinervous catheter (stimulong sono- Pajunk, Germany) will be insert between femoral nerve and femoral artery through tuohy needle (18G, 100mm length) under ultrasound guidance.
PROCEDURESpinal AnesthesiaSpinal anesthesia will be perform at L3-L4 or L4-L5 level. Levobupivacaine 0,5% 12mg will be injected.
PROCEDURELocal anesthetic infusionContinuous infusion of levobupivacaine 0,125% at 8ml/h rate through perinervous catheter until 5th postoperative day.
PROCEDUREIntravenous analgesiaKetorolac 30mg 3 times/day and morphine Patients Control Analgesia (1mg/h, max 4mg/h) administered.
DRUGRopivacaine 0,75%
DRUGLevobupivacaine 0,5%
DRUGLevobupivacaine 0,125%
DRUGKetorolac 30mg
DRUGMorphine
DEVICEstimulong sono, Pajunk, Germany

Timeline

Start date
2014-03-01
Primary completion
2015-09-01
Completion
2016-03-01
First posted
2014-03-10
Last updated
2016-08-09

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT02082067. Inclusion in this directory is not an endorsement.