Modelling Interface Pressure Applied by Superimposed Compression Bandages

THUASNE

Status: Completed

Conditions: Risk of Venous Thrombosis

Treatments: Other: Compression bandages application and interface pressure measurements

Study type: Interventional

Funder types: Industry

Identifiers

NCT02803398

2015-A01219-40

Details and patient eligibility

About

The aim of the study is to measure and model interface pressure applied on the lower leg of patients at risk of veinous thrombosis, by different bandage combinations, composed of Biflex 16 (Thuasne) and/or Rosidal K (Lohmann & Rauscher). The patient specific model should better predict the interface pressure distribution than Laplace's Law.

Full description

The measurement of the patients' legs shapes will be performed thanks to an optical scanner. The patients' posterior part of the calf will be submitted to a localized compression test, in order to characterize the soft tissue mechanical properties of both legs.

Pressure measurements, applied by the different bandages, will be taken at the height of measurement points B1 and C on the lateral and medial sides of the leg in supine, sitting and standing positions, on both legs.

2 single bandages (Biflex 16 (Thuasne) and Rosidal K (Lohmann & Rauscher)) and their different combinations will be applied on the patient's legs.

The order of bandage application for each patient is randomized, but is the same for both legs. The order of the leg (right or left) on which the bandages are applied is randomized.

Enrollment: 26 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female between 18 and 80 years old
• at risk of venous thrombosis, who need to wear compression (socks, stockings or bandage)
• Hospitalized in the Service of Physical Medicine and Rehabilitation, in Saint-Etienne, France
• BMI between 20 and 35
• Able to stand for at least 10 minutes in a standing frame
• Signed informed consent to take part in the study
• Covered by a health insurance system
• Not taking part in another study which interfere with the results of the present study

Exclusion criteria

• Compression bandages contraindications
• Allergy to one of the different bandages components
• History of deep or superficial vein thrombosis
• Venous or arterial ulcer
• Cutaneous wound on the lower leg
• Cognitive, behavior or physical disorder preventing the communication and the active participation to a rehabilitation program, or a clinical study
• Patient under any legal protection (except curatorship)
• Not covered by a health insurance system

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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26 participants in 1 patient group

Patient at risk of venous thrombosis

Experimental group

Treatment:

Other: Compression bandages application and interface pressure measurements