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Clinical Trials/NCT04507724
NCT04507724
Completed
Not Applicable

The Use of Biochemical Analyzes to Monitor the Development of Wounds: Part 1: Analysis of Wounds Without VAC Therapy: Part 2: Analysis of Wound Fluids Under VAC Therapy

Qualizyme Diagnostics GmbH & Co KG1 site in 1 country41 target enrollmentOctober 19, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Wound
Sponsor
Qualizyme Diagnostics GmbH & Co KG
Enrollment
41
Locations
1
Primary Endpoint
Part 2: Descriptive assessment of the feasibility of collecting wound fluid during ongoing negative pressure wound therapy
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Chronic wounds represent a growing challenge in medical care.

Part 1: The aim of this part of the study was to collect wound swabs and to answer the question whether the rapid diagnostic tool using enzyme activities can display an infection prematurely. This means that an increased enzyme activity (especially MPO, NHE, LYS, gelatinase, pH) measured overed 3 days, would indicate a change in the wound bed (infection, Inflammation) earlier than the regularly performed clinical assessment.

Part 2: The aim of this part of the study was to evaluate (I) the possibility of wound fluid acquisition by means of an "additional collector" during ongoing NPWT and to answer if (II) this secretion can be biochemically analyzed for enzyme activities in order to be able to detect a change in the wound situation at an early stage.

Detailed Description

The study is composed of two parts, which run independently of each other. However, in both parts the course of the wounds is analyzed. Part 1: Two wound swabs are taken. One used for routinely performed microbiological analysis and the second will be used for biochemical analysis (enzyme activities). The aim of the wound swabs is to answer the question whether the rapid diagnostic tool used in the examination can display an infection prematurely or not. This means that an increased enzyme activity (especially MPO, NHE, LYS, gelatinase, pH) would indicate a change in the wound bed (infection, inflammation) earlier than the regular clinical assessment. These wound swabs are expected to function as an improvement of the biochemical assays or rather of the technology concerning sensitivity and specificity of, for example, the pH number, the MPO, the LYS, the gelatinase and the elastase. In addition to that, the correlation between the Enzyme activities and the course of the infection will be examined. This technology is supposed to be later used as an early infection diagnostic tool in wound fluids. The followup of this testing system is a crucial prerequisite for the application of the technology in VAC therapy (part 2). Part 2: The findings of this examination will be used to investigate the applicability of the developed in-vitro early infection diagnostic tool in negative-pressure therapy (VAC therapy; vacuum assisted closure). Patients of the plastic surgery with a NPWT are included in this prospective study. Before the NPWT will be applied, two swabs (biochemical and microbiological analysis) of the wounds will be taken. After installation of the dressing, the connecting tube between the wound and the vacuum-generating device will be cut and an "additional collector" will be inserted. This collector will be changed daily and afterwards the concentrations of enzymes (lysozyme, elastase, myeloperoxidase) will be biochemically analyzed.

Registry
clinicaltrials.gov
Start Date
October 19, 2018
End Date
December 31, 2020
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christina Helene Wolfsberger

Sub-Investigator

Medical University of Graz

Eligibility Criteria

Inclusion Criteria

  • signed informed consent
  • older than 18 years old
  • open wound of varying etiology
  • VAC therapy (KCI) (part 2)

Exclusion Criteria

  • under 18 years old
  • pregnant women
  • less than three measurement data (less than three swabs) = part 1
  • VAC-instill therapy = part 2

Outcomes

Primary Outcomes

Part 2: Descriptive assessment of the feasibility of collecting wound fluid during ongoing negative pressure wound therapy

Time Frame: during negative pressure wound therapy

The aim is to answer the question if it is feasible to collect wound fluid during ongoing negative pressure wound therapy and analyze this wound fluid biochemically.

Part 1: biochemical analysis of wounds

Time Frame: during hospitalization

Elevated enzyme activities (biochemical analysis of wound swabs) give information of the condition of the wound bed (infection, inflammation).

Secondary Outcomes

  • Part 2: Evaluating changes in enzyme activities in the collected wound fluid(Starting immediately after installation of the negative-pressure dressing and lasting for 3 days.)

Study Sites (1)

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