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Clinical Trials/NCT03032133
NCT03032133CompletedNot Applicable

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

Technische Universität Dresden2 sites in 1 country140 target enrollmentStarted: February 2016Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
140
Locations
2
Primary Endpoint
pain
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Indication to Total Knee Arthroplasty
  • •Signed informed consent

Exclusion Criteria

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

Arms & Interventions

Regional pain control

Active Comparator

Regional pain catheter

Intervention: Regional pain control (Procedure)

Local pain control

Experimental

Local intraarticular pain catheter

Intervention: Local pain control (Procedure)

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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