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Local Anesthetics After Total Knee Arthroplasty

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified July 2007 by Hvidovre University Hospital.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00518674
First Posted: August 21, 2007
Last Update Posted: August 21, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Hvidovre University Hospital
August 20, 2007
August 21, 2007
August 21, 2007
January 2007
Not Provided
Visual Analogue Scale pain score
Same as current
No Changes Posted
Not Provided
Not Provided
Not Provided
Not Provided
 
Local Anesthetics After Total Knee Arthroplasty
Local Anesthetics After Total Knee Arthroplasty: Intra- vs. Extraarticular Administration? A Randomized, Double-Blind, Placebo-Controlled Study
The aim of this randomized, double-blind and placebo-controlled study is to evaluate the specific role of injection of local anesthetic into the intra- vs. extraarticular tissues after toal knee arthroplasty.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Postoperative Pain
Procedure: local infiltration analgesia
local wound infiltration with 30 ml ropivacaine 0.2 % (60 mg)
Not Provided
Andersen LØ, Kristensen BB, Madsen JL, Otte KS, Husted H, Kehlet H. Wound spread of radiolabeled saline with multi- versus few-hole catheters. Reg Anesth Pain Med. 2010 Mar-Apr;35(2):200-2.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
32
September 2007
Not Provided

Inclusion Criteria:

  • Able to give informed oral and written consent to participate
  • Able to speak Danish

Exclusion Criteria:

  • Treatment with opioids
  • Body Mass Index > 40
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
 
NCT00518674
KF01329190
No
Not Provided
Not Provided
Not Provided
Hvidovre University Hospital
Not Provided
Principal Investigator: Lasse Andersen, MD Hvidovre University Hospital, Copenhagen, Denmark
Hvidovre University Hospital
July 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP