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Clinical Trials/NCT01191593
NCT01191593
Completed
Phase 4

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

Rigshospitalet, Denmark1 site in 1 country36 target enrollmentSeptember 2010
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ConditionsPostoperative PainKnee Arthroplasty

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Rigshospitalet, Denmark
Enrollment
36
Locations
1
Primary Endpoint
Pain during 45 degrees active flexion of the knee
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to determine whether Adductor-Canal-Blockade is effective at reducing pain and morphine consumption after revision knee arthroplasty.

Registry
clinicaltrials.gov
Start Date
September 2010
End Date
April 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pia Jaeger

M.D.

Rigshospitalet, Denmark

Eligibility Criteria

Inclusion Criteria

  • •Revision Knee Arthroplasty in general anaesthesia
  • •American society of anesthesiologists (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

Outcomes

Primary Outcomes

Pain during 45 degrees active flexion of the knee

Time Frame: 4 hours postoperative

0-100 mm at a visual analogue scale (VAS), at 4 hours postoperative.

Secondary Outcomes

  • Pain during 45 degrees active flexion of the knee(24 hours postoperative)
  • Pain during rest(24 hours postoperative)
  • Total morphine consumption(0-24 hours postoperative)
  • Postoperative nausea(24 hours postoperative)
  • Postoperative vomiting(0-24 hours postoperative)
  • Zofran consumption(0-24 hours postoperative)
  • Sedation(24 hours postoperative)

Study Sites (1)

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