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The Efficacy of Adductor-Canal-Block (ACB) in Patients After Anterior Cruciate Ligament (ACL) Reconstruction

G

Glostrup University Hospital, Copenhagen

Status and phase

Completed
Phase 4

Conditions

Anterior Cruciate Ligament Reconstruction

Treatments

Procedure: Ropivacain
Procedure: Saline

Study type

Interventional

Funder types

Other

Identifiers

NCT01212666
SM1-ME-10

Details and patient eligibility

About

The Purpose of this study is to determine whether Adductor-Canal-Block is superior to placebo when it comes to analgetic efficacy after reconstruction of the anterior cruciate ligament.

Enrollment

50 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-70 years
  • Reconstruction of Anterior Cruciate Ligament
  • Written consent
  • ASA I-II
  • BMI 19-35

Exclusion criteria

  • Unable to communicate in Danish
  • Allergic reactions toward drugs used in the trial
  • Pregnancy
  • Abuse of alcohol/drugs
  • Daily opioid intake
  • Infection at injection site
  • Can not be mobilised to 5 meters of walk; pre-surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

50 participants in 2 patient groups, including a placebo group

Adductor-Canal-Block, Ropivacain
Experimental group
Description:
25 patients. ACB. 30 mL Ropivacain 7,5 mg/mL. Ultrasound-guided application.
Treatment:
Procedure: Ropivacain
Adductor Canal Block, Placebo (saline)
Placebo Comparator group
Description:
25 patients. ACB. 30 mL Saline. Ultrasound-guided application.
Treatment:
Procedure: Saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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