Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-01-31

Study Completion Date

2007-05-31

Brief Summary

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

Detailed Description

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

Conditions

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Total Knee Arthroplasty

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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compression bandage

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* scheduled for total knee arthroplasty
* speak and understand Danish

Exclusion Criteria

* severe obesity
* allergies to local anaesthetics

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Lasse Andersen, MD

Role: PRINCIPAL_INVESTIGATOR

Hvidovre University Hospital

Locations

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Hvidovre Hospital

Hvidovre, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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KF01327078

Identifier Type: -

Identifier Source: org_study_id