Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty

This study has been completed.

Sponsored by:	Hvidovre University Hospital
Information provided by:	Hvidovre University Hospital
ClinicalTrials.gov Identifier:	NCT00485212

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 IV

MedlinePlus related topics: Knee Replacement

Study Type:	Interventional
Study Design:	Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:	The Effect of a Compression Bandage in Local Infiltration Analgesia After Total Knee Arthroplasty

Further study details as provided by Hvidovre University Hospital:

Primary Outcome Measures:

Detailed Description:

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

Eligibility

Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Exclusion Criteria:

Contacts and Locations

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

Locations

Sponsors and Collaborators

Hvidovre University Hospital

Investigators

Principal Investigator:

Lasse Andersen, MD

Hvidovre Hospital

More Information

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

Keywords provided by Hvidovre University Hospital:

postoperative pain

Study placed in the following topic categories:

Pain
Pain, Postoperative

ClinicalTrials.gov processed this record on January 16, 2009