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Clinical Trials/NCT01261897
NCT01261897
Completed
Phase 4

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

Rigshospitalet, Denmark1 site in 1 country40 target enrollmentJanuary 2011

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Rigshospitalet, Denmark
Enrollment
40
Locations
1
Primary Endpoint
Pain during 45 degrees active flexion of the knee
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The objective of this study is to assess the efficacy of Adductor-Canal-Blockade on pain and morphine consumption after total knee arthroplasty. Our hypothesis is that the Adductor -Canal-Blockade is superior to placebo in reducing pain and morphine consumption after total knee arthroplasty.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
September 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pia Jaeger

MD

Rigshospitalet, Denmark

Eligibility Criteria

Inclusion Criteria

  • Total Knee Arthroplasty in general anaesthesia
  • 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

Outcomes

Primary Outcomes

Pain during 45 degrees active flexion of the knee

Time Frame: 1 hour postoperative

0-100 mm at a visual analogue scale (VAS), at 1 hour postoperative

Secondary Outcomes

  • Pain during 45 degrees active flexion of the knee(0-6 hours postoperative)
  • Pain during rest(1-6 hours postoperative)
  • A change in pain score in the ropivacaine group, after activating the block(30-60 minutes postoperative)
  • Total morphine consumption(30 minutes - 6 hours postoperative)
  • Postoperative nausea(1-6 hours postoperative)
  • Postoperative vomiting(1-6 hours postoperative)
  • Zofran consumption(1-6 hours postoperative)
  • Sedation(1-6 hours postoperative)

Study Sites (1)

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