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Clinical Trials/NCT03032133
NCT03032133
Completed
Not Applicable

Pain After Total Knee Arthroplasty With Either Regional or Local Pain Katheter

Technische Universität Dresden1 site in 1 country140 target enrollmentFebruary 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Technische Universität Dresden
Enrollment
140
Locations
1
Primary Endpoint
pain
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Patients are randomized to receive pain control after Total Knee Arthroplasty with either a regional pain catheter or a local intraarticular pain catheter. Pain, analgetic use and mobility is asessed.

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
December 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Indication to Total Knee Arthroplasty
  • Signed informed consent

Exclusion Criteria

  • Chronic pain
  • Allergy against local anaesthetics
  • Not understanding study or questionnaires

Outcomes

Primary Outcomes

pain

Time Frame: daily until day 7 after surgery

Pain on Visual Analog Scale

Secondary Outcomes

  • analgetics(daily until day 7 after surgery)
  • Mobility(daily until day 7 after surgery)
  • Function(preoperative, 3 month, 1 year)
  • Patient reported outcome(preoperative, 3 month, 1 year)
  • Quality of Life(preoperative, 3 month, 1 year)

Study Sites (1)

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