Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty

This study has been completed.

Sponsor:

Information provided by:

Hvidovre University Hospital

ClinicalTrials.gov Identifier:

NCT00485212

First received: June 11, 2007

Last updated: NA

Last verified: May 2007

History: No changes posted

Purpose

purpose: to determine wether a compression bandage prolongs analgesia of local infiltration analgesia after total knee arthroplasty

Condition	Intervention	Phase
Total Knee Arthroplasty	Device: compression bandage	Phase 4


Study Type:	Interventional
Study Design:	Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment
Official Title:	The Effect of a Compression Bandage in Local Infiltration Analgesia After Total Knee Arthroplasty

Resource links provided by NLM:

MedlinePlus related topics: Knee Replacement

U.S. FDA Resources

Further study details as provided by Hvidovre University Hospital:

Primary Outcome Measures:

pain, Visual Analogue Scale


Enrollment:	48
Study Start Date:	January 2007
Study Completion Date:	May 2007

Detailed Description:

patients are randomised to receive a compression bandage or a non-compression bandage

Eligibility


Ages Eligible for Study:	Child, Adult, Senior
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

scheduled for total knee arthroplasty
speak and understand Danish

Exclusion Criteria:

severe obesity
allergies to local anaesthetics

Contacts and Locations

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00485212

Locations


Denmark
Hvidovre Hospital
Hvidovre, Denmark, 2650

Sponsors and Collaborators

Hvidovre University Hospital

Investigators


Principal Investigator:	Lasse Andersen, MD	Hvidovre University Hospital

More Information


ClinicalTrials.gov Identifier:	NCT00485212 History of Changes
Other Study ID Numbers:	KF01327078
Study First Received:	June 11, 2007
Last Updated:	June 11, 2007
Health Authority:	Denmark: The Regional Committee on Biomedical Research Ethics

Keywords provided by Hvidovre University Hospital:


postoperative pain

ClinicalTrials.gov processed this record on September 26, 2016

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