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- Klinische Studie NCT03576989
Einfluss der oralen Therapie mit Omega-3-Fettsäuren auf die Heilung von chronischen venösen Beingeschwüren bei älteren Erwachsenen
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Die Pathogenese der CVLU umfasst eine hohe Anzahl aktivierter polymorphkerniger Leukozyten (PMN), die mit einer anhaltenden Entzündung im Wundbett einhergehen. Die vorgeschlagene Forschung soll die Wirksamkeit einer oralen Nährstoffintervention testen, die die bioaktiven Komponenten von Fischöl (Eicosapentaensäure - EPA + Docosahexaensäure - DHA) enthält, um die PMN-Aktivität zu lindern und die Heilung zu fördern. In die Studie sollen 248 aufeinanderfolgende teilnahmeberechtigte Erwachsene ≥ 55 Jahre mit CVLUs eingeschlossen werden, die weiterhin die Standardversorgung in zwei ambulanten Wundkliniken der Universität erhalten. Die Teilnehmer werden in 2 Gruppen randomisiert: 12 Wochen tägliche orale Therapie mit EPA+DHA (1,87 g/d EPA + 1,0 g/d DHA) oder tägliche orale Therapie mit Placebo. In den Wochen 0, 4, 8 und 12 werden in den beiden Gruppen drei spezifische Ziele verfolgt:
Ziel 1. Vergleich der Konzentrationen von EPA+DHA-abgeleiteten Lipidmediatoren und entzündlichen Zytokinen in Blut und CVLU-Flüssigkeit.
Unterziel 1a. Vergleichen Sie die entzündliche Zytokin-Genexpression durch PMNs im Blut (Neutrophile und Monozyten).
Ziel 2. Vergleich der PMN-Aktivierung (Blut, CVLU-Flüssigkeit) und der PMN-abgeleiteten Proteasespiegel (CVLU-Flüssigkeit).
Ziel 3. Vergleich der Verringerung der Wundfläche unter Kontrolle der Schlüsselfaktoren, von denen bekannt ist, dass sie die Heilung beeinflussen, und Bestimmung der Beziehungen zu Lipidmediatoren, Zytokinen und PMN-Aktivierung.
Unterziel 3a. Vergleichen Sie die Häufigkeit des Wiederauftretens von CVLU und die Werte der Studienvariablen im Blut zwischen 2 Untergruppen innerhalb der EPA+DHA-Gruppe mit geheilten CVLUs (nach 3 zusätzlichen Monaten EPA+DHA-Therapie versus Placebo-Therapie über den Zeitpunkt der 12. Woche hinaus).
Unterziel 3b. Vergleichen Sie das Schmerzsymptom zu allen Zeitpunkten und die Lebensqualität beim ersten und letzten Studienbesuch in den 2 Gruppen und 2 Untergruppen.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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Ohio
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Columbus, Ohio, Vereinigte Staaten, 43210
- The Ohio State University College of Nursing
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Beschreibung
Einschlusskriterien:
Frauen und Männer ≥ 55 Jahre mit:
- Ein seit mindestens 4 Wochen, aber nicht länger als 12 Monate bestehendes ZVLU zwischen Sprunggelenk und Knie, verordnete Kompressionstherapie mit 1-4-lagigem Verband;
- Knöchel-Arm-Druckindex (ABPI) zwischen 0,7 und 1,2;
- Zielbereich der Wunde von 2-60 cm2 wer kann
- Lesen und verstehen Sie Englisch oder Spanisch und
- Zustimmung geben.
Ausschlusskriterien:
- Fischallergie;
- Kortikosteroide oder selektive Cyclooxygenase (COX)-2-Hemmer (z. B. Celebrex); nichtsteroidale Antirheumatika (NSAR) > 2x/Woche (Ausnahme: Aspirin 81 mg/Tag);
- Autoimmunerkrankungen;
- Chemotherapie innerhalb von 6 Monaten nach Woche 0;
- Diabetes, wenn HbA1c > 12 % oder Geschwür, kompliziert durch Zellulitis, freiliegende Sehnen oder Knochen.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Verdreifachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: EPA+DHA-Gruppe
12 Wochen tägliche orale Therapie mit EPA+DHA (drei undurchsichtige Weichkapseln für eine tägliche Gesamtaufnahme von 1,87 g EPA + 1,0 g DHA)
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EPA+DHA sind die mehrfach ungesättigten n-3-Fettsäuren, die in Fischöl enthalten sind
Andere Namen:
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Placebo-Komparator: Placebo-Gruppe
12 Wochen tägliche orale Therapie mit Placebo (drei undurchsichtige Weichkapseln für eine tägliche Gesamtaufnahme von 2,5 ml Mineralöl)
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Placebo enthält Mineralöl
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
Zeitfenster: 0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE5 measured in pg/mL at Weeks 4, 8 and 12. 5-HEPE (5-hydroxy-eicosapentaenoic acid) is an eicosanoid derived from eicosapentaenoic acid (EPA) via the 5-lipoxygenase pathway.
It functions as an anti-inflammatory lipid mediator, in part through the generation of reactive oxygen species.
Plasma levels of 5-HEPE (also known as HEPE5) were measured using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE11
Zeitfenster: 0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE11 measured in pg/mL at Weeks 4, 8 and 12. 11-HEPE (11-hydroxy-5Z,8Z,12E,14Z,17Z-eicosapentaenoic acid) is a monohydroxy fatty acid derived from eicosapentaenoic acid (EPA).
In research, it is commonly studied as a lipid mediator (eicosanoid) associated with anti-inflammatory processes.
Plasma levels of 11-HEPE (also known as HEPE11) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE12
Zeitfenster: 0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE12 at Weeks 4, 8 and 12. 12-HEPE (12-hydroxyeicosapentaenoic acid) is an omega-3 fatty acid metabolite formed from eicosapentaenoic acid (EPA) via the 12-lipoxygenase pathway.
It functions as a signaling lipid that helps mediate the beneficial effects of EPA and exhibits potent anti-inflammatory properties.
Plasma levels of 12-HEPE (HEPE12) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE15
Zeitfenster: 0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE15 measured in pg/mL at Weeks 4, 8 and 12. 15-HEPE (15-hydroxyeicosapentaenoic acid) is an anti-inflammatory metabolite produced from the omega-3 fatty acid eicosapentaenoic acid (EPA) via the 15-lipoxygenase pathway.
It functions as a pro-resolving lipid mediator, contributing to the resolution of inflammation.
Plasma levels of 15-HEPE (HEPE15) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE18
Zeitfenster: 0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE18 measured in pg/mL at Weeks 4, 8 and 12. 18-HEPE (18-hydroxyeicosapentaenoic acid) is an anti-inflammatory metabolite of the omega-3 fatty acid eicosapentaenoic acid (EPA) and serves as a precursor for E-series resolvins.
E-series resolvins actively terminate inflammatory responses, promote the resolution of inflammation, and support tissue repair.
They exert potent anti-inflammatory effects by limiting neutrophil infiltration and suppressing pro-inflammatory cytokine production.
Plasma levels of 18-HEPE (HEPE18) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Comparison of Intervention and Control Groups in IL-1β Levels (Log pg/mL)
Zeitfenster: 0, 4, 8 and 12 weeks
|
Plasma levels of IL-1β were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma IL-1β levels expressed as log-transformed concentrations (pg/mL). The IL-1β data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in IL-1β levels. |
0, 4, 8 and 12 weeks
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Comparison of Intervention and Control Groups in IL-6 Levels (Log pg/mL)
Zeitfenster: 0, 4, 8 and 12 weeks
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Plasma levels of IL-6 were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma IL-6 levels expressed as log-transformed concentrations (pg/mL). The data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in IL-6 levels. |
0, 4, 8 and 12 weeks
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1. Comparison of Intervention and Control Groups in TNF-α Levels (Log pg/mL)
Zeitfenster: 0, 4, 8 and 12 weeks
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Plasma levels of TNF-α were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma TNF-α levels expressed as log-transformed concentrations (pg/mL). The data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in TNF-α levels. |
0, 4, 8 and 12 weeks
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Comparison of Intervention and Control Groups in IFN-γ Levels (Log pg/mL)
Zeitfenster: 0, 4, 8 and 12 weeks
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Plasma levels of IFN-γ were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma IFN-γ levels expressed as log-transformed concentrations (pg/mL). The data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in IFN-γ levels. |
0, 4, 8 and 12 weeks
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) Activation (Log Cells/µL)
Zeitfenster: 0, 4, 8 and 12 weeks
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Reported values reflect PMN activation in plasma, expressed as log-transformed concentrations (cells/µL) at Weeks 4, 8, and 12.
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0, 4, 8 and 12 weeks
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) - Derived Matrix Metalloproteinase-8 (MMP-8) Levels (Log pg/mg) in Wound Fluid
Zeitfenster: 0, 4, 8 and 12 weeks
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MMP-8, also known as neutrophil collagenase, is an enzyme that degrades collagen types I, II, and III and contributes to tissue remodeling and inflammatory processes.
Wound fluid levels of MMP-8 were quantified using the MMP-8, neutrophil collagenase, Biotrak enzyme-linked immunosorbent assay kit (GE Healthcare Bio-Sciences Corp., Piscataway,NJ).
Reported values reflect wound fluid MMP-8 levels, expressed as log-transformed concentrations (pg/mg) at Weeks 0, 4, 8, and 12.
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0, 4, 8 and 12 weeks
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) - Derived Human Neutrophil Elastase (HNE, ELA2) Levels (Log pg/mg) in Wound Fluid
Zeitfenster: 0, 4, 8 and 12 weeks
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HNE is a potent serine protease stored in neutrophil granules that plays a key role in degrading bacteria and host tissue during inflammatory responses.
Wound fluid levels of HNE were quantified using the InnuozymeTM Human Neutrophil Elastase Immunocapture Activity Assay Kit (Calbiochem, EMD Biosciences Inc., San Diego, CA).
Reported values reflect wound fluid HNE levels, expressed as log-transformed concentrations (pg/mg) at Weeks 0, 4, 8 and 12.
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0, 4, 8 and 12 weeks
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Comparison of Intervention vs. Control Groups in the Percent Change in Wound Area Relative to Baseline
Zeitfenster: 0, 4, 8 and 12 weeks
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Percentage Area Reduction (PAR) is a valuable, widely used metric for evaluating and comparing the effectiveness of wound healing interventions in research. PAR was calculated at each follow-up time point (Weeks 4, 8, and 12) relative to the baseline. It represents the percentage change in wound size (area in cm2) from baseline, computed as: "PAR"=("Baseline Area" -"Follow-up Area" )/"Baseline Area" ×100 Positive PAR values indicate a reduction in wound area (i.e., healing), whereas negative values indicate an increase in wound size compared to baseline (i.e., the wound has enlarged). |
0, 4, 8 and 12 weeks
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
Zeitfenster: 0, 12 weeks
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The VEINES-QOL/Sym questionnaire consists of 26 items designed to assess both disease-specific quality of life (VEINES-QOL) and symptom severity (VEINES-Sym) in individuals with venous disorders.
The instrument evaluates two separate metrics, both of which are calculated using the mean of standardized z-scores.
The typical theoretical range for both is roughly 0 to 100, with a mean population standard of 50.
The final score was calculated after calculating the mean of all z scores, which were multiplied by 10, and then added to 50.
Higher scores indicate better quality of life and fewer symptoms (i.e., a more favorable outcome).
VEINES-QOL/Sym scores are expressed as Z-scores standardized to a reference population, with a mean of 0 and standard deviation of 1.
A Z-score of 0 represents the population mean.
Higher Z-scores indicate better quality of life and fewer venous insufficiency symptoms, while lower Z-scores indicate worse outcomes.
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0, 12 weeks
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Venous Clinical Severity Score (VCSS)
Zeitfenster: 0, 4, 8, 12 weeks
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The Venous Clinical Severity Score (VCSS) is a 10-item, 30-point scoring system used to assess and track the severity of chronic venous disease (CVD) and its response to treatment, ranging from 0 (none) to 3 (severe) for parameters like pain, ulcers, and edema.
Scores can range from 0 to 30 with higher scores meaning more severe venous disease.
The average scores at Weeks 0, 4, 8 and 12 were calculated for each treatment group.
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0, 4, 8, 12 weeks
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Jodi C McDaniel, PhD, Ohio State University, College of Nursing
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Hautkrankheiten
- Hautgeschwür
- Haut- und Bindegewebserkrankungen
- Beingeschwür
- Wunden und Verletzungen
- Organische Chemikalien
- Fettsäuren
- Lipide
- Kohlenwasserstoffe
- Eicosanoide
- Fettsäuren, ungesättigt
- Öle
- Nahrungsfette
- Fette
- Fettsäuren, Omega-3
- Diätetische Fette, ungesättigt
- Petrolatum
- Mineralöl
- Eicosapentaensäure
- Docosahexaensäuren
- Fischöle
Andere Studien-ID-Nummern
- 2018H0261
- R01AG059981 (US NIH Stipendium/Vertrag)
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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