- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03576989
Indvirkning af oral terapi med omega-3 fedtsyrer på heling af kroniske venøse bensår hos ældre voksne
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Patogenesen af CVLU involverer et højt antal af aktiverede polymorfonukleære leukocytter (PMN), der er forbundet med vedvarende betændelse i sårbunden. Den foreslåede forskning skal teste effektiviteten af en oral, næringsintervention, der indeholder de bioaktive komponenter i fiskeolie (eicosapentaensyre - EPA + docosahexaensyre - DHA) for at dæmpe PMN-aktivitet og fremme heling. Undersøgelsen planlægger at inkludere 248 successive berettigede voksne ≥ 55 år med CVLU'er, som fortsætter med at modtage standardbehandling på to universitets ambulante sårklinikker. Deltagerne vil blive randomiseret til 2 grupper: 12 ugers daglig oral terapi med EPA+DHA (1,87 g/d EPA + 1,0 g/d DHA) eller daglig oral terapi med placebo. Efter 0, 4, 8 og 12 uger, på tværs af de 2 grupper, vil tre specifikke mål blive forfulgt:
Mål 1. Sammenlign niveauer af EPA+DHA-afledte lipidmediatorer og inflammatoriske cytokiner i blod og CVLU-væske.
Delmål 1a. Sammenlign inflammatorisk cytokin-genekspression af PMN'er i blod (neutrofiler og monocytter).
Mål 2. Sammenlign PMN-aktivering (blod, CVLU-væske) og PMN-afledte proteaseniveauer (CVLU-væske).
Formål 3. Sammenlign reduktion i sårareal, kontroller for nøglefaktorer, der vides at påvirke helingen, og bestem forhold til lipidmediatorer, cytokiner og PMN-aktivering.
Delmål 3a. Sammenlign hyppigheden af CVLU-tilbagefald og niveauer af undersøgelsesvariabler i blod mellem 2 undergrupper inden for EPA+DHA-gruppen med helede CVLU'er (efter yderligere 3 måneders EPA+DHA-behandling versus placeboterapi efter tidspunktet for uge 12).
Delmål 3b. Sammenlign symptomet på smerte på alle tidspunkter og livskvalitet ved første og sidste studiebesøg på tværs af de 2 grupper og 2 undergrupper.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Ohio
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Columbus, Ohio, Forenede Stater, 43210
- The Ohio State University College of Nursing
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Beskrivelse
Inklusionskriterier:
Kvinder og mænd ≥ 55 år med:
- En CVLU mellem ankel og knæ, der har været til stede i mindst 4 uger, men ikke længere end 12 måneder, ordineret kompressionsbehandling med 1-4 lags bandagering;
- Ankel brachial trykindeks (ABPI) mellem 0,7 og 1,2;
- Mål sårareal på 2-60 cm2 hvem kan
- Læs og forstå engelsk eller spansk, og
- Giv samtykke.
Ekskluderingskriterier:
- Fiskeallergi;
- Kortikosteroider eller selektive cyclooxygenase (COX)-2-hæmmere (f.eks. Celebrex); ikke-steroide antiinflammatoriske lægemidler (NSAIDS) > 2x/uge (undtagelse: aspirin 81 mg/dag);
- Autoimmune sygdomme;
- Kemoterapi inden for 6 måneder af uge 0;
- Diabetes hvis HbA1c > 12 % eller sår kompliceret af cellulitis, blotlagt sene eller knogle.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Tredobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: EPA+DHA Group
12 ugers daglig oral behandling med EPA+DHA (tre uigennemsigtige softgels for at give et samlet dagligt indtag på 1,87 g EPA + 1,0 g DHA)
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EPA+DHA er de n-3 flerumættede fedtsyrer indeholdt i fiskeolie
Andre navne:
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Placebo komparator: Placebo gruppe
12 ugers daglig oral behandling med placebo (tre uigennemsigtige softgels for at give et samlet dagligt indtag på 2,5 ml mineralolie)
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placebo indeholder mineralolie
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 0, 4, 8 and 12 weeks
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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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
Tidsramme: 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)
Tidsramme: 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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Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Jodi C McDaniel, PhD, Ohio State University, College of Nursing
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2018H0261
- R01AG059981 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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