Evaluation of the Action of MOBIDERM® on Periarticular Edema After Total Knee Prosthesis - Randomized Controlled

Centre Hospitalier Universitaire de Nīmes44 enrolled

Overview

We hypothesize that the use of MOBIDERM® after total knee prosthesis allows a greater and faster resorption of periarticular edema: * improvement of knee flexion; * faster functional gain; * faster decrease in postoperative pain by decreasing tissue tension.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Edema Arthroplasty, Replacement, Knee

Interventions

MOBIDERMDEVICE

Use of a MOBIDERM mobilizing band after total knee prosthesis

Eligibility

Sex: ALLMin age: 18 YearsMax age: 90 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patient requiring a first total knee prosthesis (scheduled between Tuesday and Friday). * Patient that has given his/her free and informed consent and signed the consent form. * The patient must be a member or beneficiary of a health insurance plan * The patient is at least 18 years old (≥) and under 90 years old (\<). Exclusion Criteria: * The subject is in a period of exclusion determined by a previous study (therapeutic study) * The subject refuses to sign the consent * It is impossible to give the subject informed information * The patient is under safeguard of justice or state guardianship * The patient is pregnant or breastfeeding * The patient is allergic to latex bandages. * The subject has contralateral amputation, pressure ulcers, severe Obstructive Arteriopathy of Lower Limbs, lymphoedema or thromboembolic event of the lower limb (ipsilateral and / or contralateral / superficial or deep or detected by postoperative Doppler). * The subject has chronic or active wounds or any cause that hinders normal rehabilitation or the application of a bandage. * patient with a stroke / Disabling Neurological Pathology, Chronic Immunological Pathology / Systemic Disease. * patient with Hepatic insufficiency. * patient with Venous insufficiency (stages 3 and 4). * The patient is on dialysis. * The subject has cognitive or behavioral disorders (Parkinson's disease, cerebellar syndrome, opposition, agitation, dementia). * The subject has a history of knee surgery.

Locations (1)

Nîmes University Hospital

Nîmes, France

Outcomes

Primary Outcomes

Knee volume

unit: mm3

Time frame: Day -1

Knee volume

unit: mm3

Time frame: Day 0

Knee volume

unit: mm3

Time frame: Day 1

Knee volume

unit: mm3

Time frame: Day 5

Knee volume

unit: mm3

Time frame: Day 15

Knee volume

unit: mm3

Time frame: Month 1