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Continuous Adductor Canal Block for Total Knee Arthroplasty Analgesia

I

Institut Kassab d'Orthopédie

Status

Unknown

Conditions

Pain Management
Neuromuscular Blockade

Treatments

Procedure: Continuous femoral nerve block
Procedure: infragluteal Sciatic nerve block
Procedure: Continuous adductor canal block
Drug: Saline
Drug: Ropivacaine 0.2%

Study type

Interventional

Funder types

Other

Identifiers

NCT02387021
P-2015002/AR

Details and patient eligibility

About

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 .

Enrollment

80 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups

Continous femoral nerve block
Active Comparator group
Description:
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 .
Treatment:
Procedure: infragluteal Sciatic nerve block
Drug: Saline
Procedure: Continuous adductor canal block
Drug: Ropivacaine 0.2%
Procedure: Continuous femoral nerve block
Continuous adductor canal block
Experimental group
Description:
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 .
Treatment:
Procedure: infragluteal Sciatic nerve block
Drug: Saline
Procedure: Continuous adductor canal block
Drug: Ropivacaine 0.2%
Procedure: Continuous femoral nerve block

Trial contacts and locations

0

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Central trial contact

Karim Raies, M.D

Data sourced from clinicaltrials.gov

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