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Continuous Adductor Canal Block for Total Knee Arthroplasty Analgesia

Not Applicable
Conditions
Neuromuscular Blockade
Pain Management
Interventions
Procedure: Continuous femoral nerve block
Procedure: Continuous adductor canal block
Procedure: infragluteal Sciatic nerve block
Drug: Saline
Registration Number
NCT02387021
Lead Sponsor
Institut Kassab d'Orthopédie
Brief Summary

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 .

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Elective unilateral TKA,
  • Planned continuous spinal anesthesia ,
  • Ability to follow study protocol,
  • American Society of Anesthesiologists class 1 to 3.
Exclusion Criteria
  • Contraindication for neuraxial anesthetic,
  • Chronic opioid use (defined as daily or almost daily use of opioids for >3 months),
  • Hypersensitivity and/or allergies to any of the study medications,
  • Intraoperative use of volatile anesthetics,
  • Preexisting neuropathy on the operative limb,
  • Contraindications to a femoral, adductor canal or Tibial nerve block.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Continous femoral nerve blockinfragluteal Sciatic nerve blockPatients 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 .
Continous femoral nerve blockRopivacaine 0.2%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 .
Continuous adductor canal blockContinuous adductor canal blockPatients 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 .
Continous femoral nerve blockSalinePatients 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 .
Continuous adductor canal blockContinuous femoral nerve blockPatients 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 .
Continuous adductor canal blockSalinePatients 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 .
Continous femoral nerve blockContinuous femoral nerve blockPatients 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 .
Continous femoral nerve blockContinuous adductor canal blockPatients 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 .
Continuous adductor canal blockinfragluteal Sciatic nerve blockPatients 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 .
Continuous adductor canal blockRopivacaine 0.2%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 .
Primary Outcome Measures
NameTimeMethod
Total Opioid-consumption8 hours postoperative

Cumulative opioid consumption : converting oral, intravenous, and patient-controlled analgesia PCA opioid to morphine equivalent

Secondary Outcome Measures
NameTimeMethod
NRS pain score at rest0,1,2,4,6,8,12,24 and 48 hours postoperative

NRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale at rest.

NRS pain score during movement0,1,2,4,6,8,12,24 and 48 hours postoperative

NRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale, during physiotherapy.

patient satisfaction8, 24 and 48 hours postoperative

patient interviewed, using a scale of 0-10, 0 not satisfied and 10 being the most satisfied

Ability to walk8, 24 and 48 hours postoperative

The ability of the patient to stand up and walk 3 meters.

NRS pain score after 10 meters of walk or maximum walked distance8, 24 and 48 hours postoperative

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).

TUG Test8, 24 and 48 hours postoperative

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

The 10-m walk test8, 24 and 48 hours postoperative

time it takes the patient to walk a distance of 10 m as quickly as possible

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