An interventional study of Continuous femoral nerve block and Continuous adductor canal block in Neuromuscular Blockade and Pain Management, sponsored by Institut Kassab d'Orthopédie. Status unknown. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2015-03-12.
Sponsored by Institut Kassab d'Orthopédie · Not applicable, Interventional, and Treatment
The purpose of the study is to determine whether the association of sciatic nerve block to continuous adductor canal block is effective in the treatment of total knee arthroplasty post operative pain .
Institut Kassab d'Orthopédie is the lead sponsor of 4 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Patients will receive ultrasound-guided (USG) continuous femoral nerve block with 20 ml ropivacaine 0.2% and USG Continuous adductor canal block with 20 ml of saline and USG infragluteal SNB with 20 ml of saline .
Procedure: Continuous femoral nerve block · Procedure: Continuous adductor canal block · Procedure: infragluteal Sciatic nerve block · Drug: Ropivacaine 0.2% · Drug: Saline
Patients will receive ultrasound-guided continuous adductor canal block with 20 ml ropivacaine 0.2% and USG infragluteal SNB with 20 ml ropivacaine 0.2% and USG continuous FNB with 20 ml of saline .
Procedure: Continuous femoral nerve block · Procedure: Continuous adductor canal block · Procedure: infragluteal Sciatic nerve block · Drug: Ropivacaine 0.2% · Drug: Saline
Total Opioid-consumption
Cumulative opioid consumption : converting oral, intravenous, and patient-controlled analgesia PCA opioid to morphine equivalent
Time frame: 8 hours postoperative
NRS pain score at rest
NRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale at rest.
Time frame: 0,1,2,4,6,8,12,24 and 48 hours postoperative
NRS pain score during movement
NRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale, during physiotherapy.
Time frame: 0,1,2,4,6,8,12,24 and 48 hours postoperative
NRS pain score after 10 meters of walk or maximum walked distance
NRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale after 10 meters walk (if enable after maximum walked distance).
Time frame: 8, 24 and 48 hours postoperative
Ability to walk
The ability of the patient to stand up and walk 3 meters.
Time frame: 8, 24 and 48 hours postoperative
TUG Test
The TUG test measures the time it takes a patient to stand up from a chair, walk a distance of 3 m, and return to the chair
Time frame: 8, 24 and 48 hours postoperative
The 10-m walk test
time it takes the patient to walk a distance of 10 m as quickly as possible
Time frame: 8, 24 and 48 hours postoperative
patient satisfaction
patient interviewed, using a scale of 0-10, 0 not satisfied and 10 being the most satisfied
Time frame: 8, 24 and 48 hours postoperative
No study locations are listed for this record.
This study is status unknown, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.
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Institut Kassab d'Orthopédie