Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty
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ClinicalTrials.gov Identifier: NCT00485212 |
Recruitment Status
:
Completed
First Posted
: June 12, 2007
Last Update Posted
: June 12, 2007
|
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Total Knee Arthroplasty | Device: compression bandage | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 48 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | The Effect of a Compression Bandage in Local Infiltration Analgesia After Total Knee Arthroplasty |
Study Start Date : | January 2007 |
Actual Study Completion Date : | May 2007 |

- pain, Visual Analogue Scale

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Ages Eligible for Study: | Child, Adult, Senior |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- scheduled for total knee arthroplasty
- speak and understand Danish
Exclusion Criteria:
- severe obesity
- allergies to local anaesthetics

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00485212
Denmark | |
Hvidovre Hospital | |
Hvidovre, Denmark, 2650 |
Principal Investigator: | Lasse Andersen, MD | Hvidovre University Hospital |
ClinicalTrials.gov Identifier: | NCT00485212 History of Changes |
Other Study ID Numbers: |
KF01327078 |
First Posted: | June 12, 2007 Key Record Dates |
Last Update Posted: | June 12, 2007 |
Last Verified: | May 2007 |
Keywords provided by Hvidovre University Hospital:
postoperative pain |