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Femoral or Sciatic Nerve Block to Provide Analgesia After Proximal Tibial Osteotomy

V

Vaud University Hospital Center

Status

Completed

Conditions

Postoperative Pain

Treatments

Procedure: Sciatic nerve block with ropivacaine 0.5%, 20 ml
Procedure: Femoral nerve block with ropivacaine 0.5%, 20 ml

Study type

Interventional

Funder types

Other

Identifiers

NCT05728294
2018-01774

Details and patient eligibility

About

Proximal tibial osteotomy is associated with moderate to severe postoperative pain. The proximal part of the tibia is innervated by branches from the femoral nerve anteriorly and the sciatic nerve posteriorly. Little is known on the type of peripheral nerve block to perform so that optimal postoperative analgesia is provided with minimum impact on the motor function. This randomised controlled double-blinded trial tested the hypothesis that a femoral nerve block provides superior analgesia than a sciatic nerve block after proximal tibial osteotomy.

Enrollment

50 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • proximal tibial osteotomy

Exclusion criteria

  • femoral or sciatic nerve deficit,
  • pre-existing peripheral neuropathy,
  • chronic pain diagnosis,
  • pregnancy,
  • identified contraindications to peripheral nerve block (e.g., local anesthetic allergy, coagulopathy, or infection at the block site).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

Femoral nerve block
Active Comparator group
Description:
Femoral nerve block performed under ultrasound guidance with ropivacaine 0.5%, 20mL
Treatment:
Procedure: Femoral nerve block with ropivacaine 0.5%, 20 ml
Sciatic nerve block
Experimental group
Description:
Sciatic nerve block performed under ultrasound guidance with ropivacaine 0.5%, 20mL
Treatment:
Procedure: Sciatic nerve block with ropivacaine 0.5%, 20 ml

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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