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The Efficacy of Adductor-Canal-Blockade on Morphine Consumption, Pain and Mobilisation After Total Knee Arthroplasty

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Rigshospitalet

Status and phase

Completed
Phase 4

Conditions

Total Knee Arthroplasty

Treatments

Procedure: Adductor-Canal-Blockade
Procedure: Adductor-Canal-blockade with saline

Study type

Interventional

Funder types

Other

Identifiers

NCT01104883
SM1-PJ-2009
2009-017794-37 (EudraCT Number)

Details and patient eligibility

About

The purpose of this study is to determine whether Adductor-Canal-Blockade is effective at reducing morphine consumption and pain, and at the same time improving mobilisation after total knee arthroplasty.

Enrollment

70 estimated patients

Sex

All

Ages

50 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Total Knee Arthroplasty in spinal anaesthesia
  • ASA 1-3
  • BMI 18-40
  • Written informed consent

Exclusion criteria

  • Can not cooperate to the exam
  • Do not speak or understand Danish
  • Drug allergy
  • Alcohol or drug abuse
  • Daily consumption of strong opioids
  • Unable to complete the Timed Up and Go test preoperatively

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

70 participants in 2 patient groups, including a placebo group

Adductor-Canal-Blockade
Experimental group
Description:
Adductor-Canal-Blockade with ropivacaine
Treatment:
Procedure: Adductor-Canal-Blockade
Adductor-Canal-blockade with saline
Placebo Comparator group
Description:
Adductor-Canal-blockade with isotonic saline
Treatment:
Procedure: Adductor-Canal-blockade with saline

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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