Impact of a Technique of Massage During the First Week of Hospitalization on the Recycling of the Mobility of the Knee Further to the Installation of Knee Replacement
NCT ID: NCT02278627
Last Updated: 2025-08-01
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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COMPLETED
NA
44 participants
INTERVENTIONAL
2014-09-30
2017-12-31
Brief Summary
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The investigators would like to complete the physiotherapist's support with manual lymphatic drainage (MLD) using a specific method based on pressure of finger splayed (PFS). This might have a positive impact on time recovery of joint range, on postoperative oedema resorbtion and on patient's pain during rehabilitation classes.
French National Authority for Health specifies there is not a single study assessing massage effects on knee replacement, according to current bibliography.
The investigators purpose is the establishment of a prospective, controlled, randomised trial referred as a "superiority" trial. A total of 98 patients divided in 2 parallel groups will be created.
The study will be in an open-label manner for both patient and physiotherapist involved in walk rehabilitation but will be conducted as a blinded study for the investigating physiotherapist.
Inclusion period will be 17 months and the following period will be 6 weeks.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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manual lymphatic drainage
We wish to complete the physiotherapist's support with manual lymphatic drainage (MLD) using a specific method based on pressure of finger splayed (PFS)
manual lymphatic drainage
Usual treatment
No interventions assigned to this group
Interventions
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manual lymphatic drainage
Eligibility Criteria
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Inclusion Criteria
* Men and women operated for a knee replacement.
* Patients affiliated to a social security system and having given their informed consent write.
Exclusion Criteria
* Patients presenting contraindications to the administration of a treatment by héparine
* Patients affected by insane pathology or by confusion.
* Patients participating in another medical research
* Pregnant and breast-feeding women and without effective contraception.
* Patients under guardianship or guardianship.
18 Years
ALL
No
Sponsors
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University Hospital, Limoges
OTHER
Responsible Party
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Locations
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University Hospital, Limoges
Limoges, , France
Countries
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Other Identifiers
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I11002
Identifier Type: -
Identifier Source: org_study_id
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