Quantification of the Pressure Threshold Related to Tissue Injury in Bedriden Paraplegics

The aim of this study is to correlate the intensity and the duration of a mechanical strain, applied over the skin of a bedridden paraplegics, with the microvascularization parameters (oxygen saturation, blood flow and blood volume) and the early inflammatory mechanism. We want to detect the early stage of irreversible damage for each patient. To achieve this goal, we measure some specifics data over a group of 48 paraplegics admitted in the hospital for a pressure ulcer surgical treatment. The patients are randomly distributed in 4 groups. First the interface pressure between the patient body and the air mattress is recorded continuously for 3 hours (= the repositioning patient frequency): we have the pressure over each point of the patient body in contact with the mattress on this time lap. Then, we will measure the microvascularization parameters, using an O2C medical device over a trochanter on a specific anatomical area which will be thereafter biopsied. Finally, depending on the group in which they were randomly distributed, the patient will undergo a muscle biopsy on his or her trochanter at 0h, 1h, 2h or 3h after they lie down on the air mattress. This way, we will be able to determine the effect of the mechanical strain duration on the physiologic parameters. The following day, the patient is undergoing his or her surgery for removing the necrotic area of the bedsore. At the same time, we will recover some of the sample near the bedsore which would serve as a maximum inflammatory response. Then a second muscle biopsy will be performed on an innervated area to be able to determine a basal concentration of biomarkers.

The inclusion period for this study will be 3 years. All the patients are followed for 24 hours then they will be followed by medical staff in their bedsore resection setting.

The data gained for this study will hopefully help the scientific world to achieve a better understanding of the pressure ulcer aetiology. They will also be helpful to achieve a mobilization of the patient specific of his or her inherent characteristics with a high sensitivity level. This way we will have a more efficient bedsore prevention.

Study Overview

• Status: Terminated
• Conditions: Spinal Cord Injury; Pressure Ulcer; Paraplegia; Bedsore
• Intervention / Treatment: Procedure: Muscle biopsy

• Study Type: Interventional
• Enrollment (Actual): 21
• Phase: Not Applicable

Contacts and Locations

Study Locations

• France
  • Montpellier, France, 34295
    • CHU Montpellier

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 90 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Educated consent signed,
• Older than 18,
• Paraplegia for at least 6 months,
• Patient's Body Mass Index > 18,5kg/m²,
• Surgery planned for pressure ulcer resection,
• Pressure Ulcer classification (EPUAP) at least III or IV

Exclusion Criteria:

• Cardiac pathology,
• Duchenne muscular dystrophy,
• Dementia,
• Presence of a tumourous wound,
• Stade IV arteritis non-revascularisable,
• Diabetes mellitus,
• Cachexia,
• Impossibility to stop the anti-coagulant treatment 24 hours before the patient admission,
• Xylocaine allergy,
• Patient took aspirin or anti-inflammatory 3 days before the biopsy,
• Patient taking part in another study,
• Patient with no health insurance,
• Pregnant women or breast-feeding, patient unable to give his or her educated consent, ward of the state (art. L.1121-6, L.1121-7, L.1211-8, L.1211-9)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Time of the first biopsy: H0; For the patients in arm H0, the first biopsy is done as soon as the patient is lying on the air mattress.	Procedure: Muscle biopsy
Active Comparator: Time of the first biopsy: H1; For a patient in arm H1, it is done after 1 hour lying on the air mattress.	Procedure: Muscle biopsy
Active Comparator: Time of the first biopsy: H2; For a patient in arm H2, it is done after 2 hour lying on the air mattress.	Procedure: Muscle biopsy
Active Comparator: Time of the first biopsy: H3; For a patient in arm H3, it is done after 3 hour lying on the air mattress.	Procedure: Muscle biopsy

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
The interface pressure will be continuously assessed using a mapping device (XSensor) during 3 hours.	The first day of the patient admission (during the first 3 hours).

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The microvascularization changes underneath the compressed skin and the inflammatory response of the muscle cells.	The blood flow, the oxygen saturation and the hemoglobin amount will be measured using a medical device called Oxygen To See (O2C). The reactive oxygen species or ROS and other specific biomarkers will be used to measure and quantify the inflammatory response of muscle cells.	The first day of the patient admission (during the first 3 hours).

Collaborators and Investigators

• Sponsor: University Hospital, Montpellier
• Collaborators: Hill-Rom

Study record dates

Study Major Dates

• Study Start (Actual): October 1, 2015
• Primary Completion (Actual): October 2, 2019
• Study Completion (Actual): October 2, 2019

Study Registration Dates

• First Submitted: April 3, 2015
• First Submitted That Met QC Criteria: April 7, 2015
• First Posted (Estimate): April 8, 2015

Study Record Updates

• Last Update Posted (Actual): December 23, 2021
• Last Update Submitted That Met QC Criteria: December 22, 2021
• Last Verified: December 1, 2021

More Information

Terms related to this study

• Keywords: Monitoring; Pressure ulcer; Interface pressure; Pressure mapping device; Ischemia reperfusion; Microvascularization
• Additional Relevant MeSH Terms: Central Nervous System Diseases; Nervous System Diseases; Skin Diseases; Neurologic Manifestations; Skin Ulcer; Trauma, Nervous System; Spinal Cord Diseases; Paralysis; Wounds and Injuries; Spinal Cord Injuries; Pressure Ulcer; Paraplegia
• Other Study ID Numbers: 95022