The Use of Compression Bandages in Total Knee Replacement Surgery
NCT ID: NCT02253680
Last Updated: 2014-10-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
50 participants
INTERVENTIONAL
2013-11-30
2015-08-31
Brief Summary
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The aim is to determine the feasibility of conducting a randomised control trial comparing the use of a compression bandage worn post-operatively for 24 hours after elective total knee replacement, compared to standard practice (wool and crepe, non-compressive dressing).
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Routine care
Wool and crepe bandage for 24 hours post-operatively
No interventions assigned to this group
Compression bandage
Actico, inelastic, short-stretch compression bandage worn 24 hours post-operatively
Actico, short-stretch, inelastic dressing
Worn 24hr post-operatively
Interventions
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Actico, short-stretch, inelastic dressing
Worn 24hr post-operatively
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Able to give written, informed consent
* Primary total knee replacement
Exclusion Criteria
* Lower limb neurological disorder
18 Years
ALL
Yes
Sponsors
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Northumbria Healthcare NHS Foundation Trust
OTHER
Responsible Party
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Mike Reed
Consultant Trauma and Orthopaedic Surgeon
Principal Investigators
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Mike Reed, MD FRCS
Role: PRINCIPAL_INVESTIGATOR
Northumbria NHS Trust
Locations
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Wansbeck District General Hospital
Ashington, Northumberland, United Kingdom
Northumbria Healthcare NHS Foundation Trust
Ashington, , United Kingdom
Countries
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Other Identifiers
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RCTTKR-01
Identifier Type: -
Identifier Source: org_study_id
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