MedPath

Combined Molecular and Mechanistic Methods for Detection of Pressure Ulcers

Not yet recruiting
Conditions
Pressure Ulcer
Inflammatory Response
Interventions
Procedure: non-invasive ventilation teraphy, NIV
Registration Number
NCT06468306
Lead Sponsor
Linkoeping University
Brief Summary

This project aims to develop a novel method for identifying early tissue damage related to pressure ulcer (PU) development in vulnerable patients by measuring biomarkers of inflammation on the skin surface. PUs are common and costly injuries that result from prolonged pressure on the skin. Current methods to assess PU risk are unreliable, and the mechanisms of PU development are not well understood. This project contributes to new knowledge of PU etiology as well as the individual variability at a molecular level combined with new knowledge about nursing actions and clinical factors linked to PU progression and outcomes of prevention. The project will use non-invasive techniques and model-based analysis to identify specific biomolecules that reflect individual susceptibility to pressure exposure in different PU risk scenarios.

Detailed Description

Purpose and aims A pressure ulcer (PU) is a localized injury to the skin and/or underlying tissue and develop from prolonged pressure on the skin. Such injuries are common in the healthcare setting, especially among vulnerable elderly. PUs greatly decrease the quality of life of individuals and are costly for the healthcare system. As many as 14% of the inpatients suffered from PUs in the Swedish country's municipalities and regions during 2022. The origin and timing of events leading to PUs are not fully understood, and current methods to assess the risk for an individual to develop a PU, are unreliable. Therefore, there is an urgent need to develop more objective, sensitive and specific methods for identifying early signs of tissue damage before they come visible and thus avoid development of PUs.

The investigators have previously identified a preliminary set of molecular biomarkers (cytokines and proteins), sampled non-invasively in the sebum, that reflects the inflammatory process under-pinning PU etiology and, possibly, individual susceptibility to pressure exposure. Therefore, it is hypothesize that non-invasive measurements of specific biomolecules on the skin surface, together with model-based analysis, can be used for individualized PU prediction. Accordingly, the purpose of this project is to confirm and expand on these preliminary findings in different PU risk scenarios to model the underlying inflammatory processes that reflect the individual vulnerability of the skin caused by pressure exposure and use modeling to extract a new layer of mechanistic insights of the underlying inflammatory process in different patient populations.

The specific aims of the project are:

1. To establish and validate optimal combinations of molecular biomarkers to identify individual susceptibility to pressure exposure during routine management regimes related to medical devises non-invasive ventilation (NIV) therapy.

2. To unravel key mechanisms in inflammatory processes related to early tissue damage by developing a mathematical model for the timing of events in the response to pressure, based on collected biomolecules, earlier data, and interaction databases

3. To identify risk factors of PU vulnerability on an individual level in routine clinical settings by combining biomolecules, model-based simulations, and clinical parameters

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • patients that use oronasal face masks in their ordinary care during routine management regimes of non invasive ventilation.

Exclusion Criteria

  • acute respiratory failure
  • previous ICU care
  • pressure ulcer on measurement site
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
individuals with NIV treatmentnon-invasive ventilation teraphy, NIVPatients that use oronasal face masks in their ordinary care to measure early-stage medical devise-related tissue damage during routine management regimes of NIV. Approximately 150 adult patients of both sexes will be recruited, from facilities that employ oronasal face masks in the routine care.
Primary Outcome Measures
NameTimeMethod
GM-CSF2 minutes

inflammatory biomarker

GRO-alpha2 minutes

inflammatory biomarker

I-3092 minutes

inflammatory biomarker

IL-22 minutes

inflammatory biomarker

IL-272 minutes

inflammatory biomarker

IL-32 minutes

inflammatory biomarker

IL-312 minutes

inflammatory biomarker

IL-92 minutes

inflammatory biomarker

MIP-1α2 minutes

inflammatory biomarker

ENA-782 minutes

inflammatory biomarker

IFN-α2a2 minutes

inflammatory biomarker

IFN-γ2 minutes

inflammatory biomarker

IL-152 minutes

inflammatory biomarker

IL-17E/IL-252 minutes

inflammatory biomarker

IL-232 minutes

inflammatory biomarker

IL-72 minutes

inflammatory biomarker

CTACK2 minutes

inflammatory biomarker

Eotaxin2 minutes

inflammatory biomarker

FLT3L2 minutes

inflammatory biomarker

Fractalkine2 minutes

inflammatory biomarker

Eotaxin-22 minutes

inflammatory biomarker

IL-17A2 minutes

inflammatory biomarker

IL-17A/F2 minutes

inflammatory biomarker

IL-17C2 minutes

inflammatory biomarker

IL-222 minutes

inflammatory biomarker

IL-42 minutes

inflammatory biomarker

IP-102 minutes

inflammatory biomarker

MCP-12 minutes

inflammatory biomarker

MCP-32 minutes

inflammatory biomarker

TNF-α2 minutes

inflammatory biomarker

Eotaxin-32 minutes

inflammatory biomarker

EPO2 minutes

inflammatory biomarker

IL-102 minutes

inflammatory biomarker

IL-12/IL-23p402 minutes

inflammatory biomarker

IL-12p702 minutes

inflammatory biomarker

IL-132 minutes

inflammatory biomarker

IL-162 minutes

inflammatory biomarker

IL-17B2 minutes

inflammatory biomarker

IL-17D2 minutes

inflammatory biomarker

IL-17F2 minutes

inflammatory biomarker

IL-182 minutes

inflammatory biomarker

IL-1RA2 minutes

inflammatory biomarker

IL-1α2 minutes

inflammatory biomarker

IL-1β2 minutes

inflammatory biomarker

IL-332 minutes

inflammatory biomarker

IL-52 minutes

inflammatory biomarker

MCP-42 minutes

inflammatory biomarker

M-CSF2 minutes

inflammatory biomarker

MDC2 minutes

inflammatory biomarker

MIF2 minutes

inflammatory biomarker

MIP-3β2 minutes

inflammatory biomarker

SDF-1alpha2 minutes

inflammatory biomarker

MIP-1β2 minutes

inflammatory biomarker

MIP-52 minutes

inflammatory biomarker

TRAIL2 minutes

inflammatory biomarker

TSLP2 minutes

inflammatory biomarker

VEGF-A2 minutes

inflammatory biomarker

IL-82 minutes

inflammatory biomarker

G-CSF2 minutes

inflammatory biomarker

IFN-β2 minutes

inflammatory biomarker

IL-212 minutes

inflammatory biomarker

IL-29/IFN-L12 minutes

inflammatory biomarker

IL-2Ra2 minutes

inflammatory biomarker

IL-62 minutes

inflammatory biomarker

I-TAC2 minutes

inflammatory biomarker

MCP-22 minutes

inflammatory biomarker

MIP-3α2 minutes

inflammatory biomarker

TARC2 minutes

inflammatory biomarker

TNF-β2 minutes

inflammatory biomarker

TPO2 minutes

inflammatory biomarker

YKL-402 minutes

inflammatory biomarker

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Linköping University

🇸🇪

Linköping, Sweden

© Copyright 2025. All Rights Reserved by MedPath