- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03576989
Effekten av oral terapi med omega-3 fettsyrer på helbredelse av kroniske venøse bensår hos eldre voksne
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Patogenesen til CVLU involverer et høyt antall aktiverte polymorfonukleære leukocytter (PMN) som er assosiert med vedvarende betennelse i sårbunnen. Den foreslåtte forskningen er å teste effekten av en oral, næringsintervensjon som inneholder de bioaktive komponentene i fiskeolje (eikosapentaensyre - EPA + dokosaheksaensyre - DHA) for å dempe PMN-aktivitet og fremme helbredelse. Studien planlegger å inkludere 248 påfølgende kvalifiserte voksne ≥ 55 år med CVLUer som fortsetter å motta standardbehandling ved to polikliniske sårklinikker ved universitetet. Deltakerne vil bli randomisert til 2 grupper: 12 ukers daglig oral terapi med EPA+DHA (1,87 g/d EPA + 1,0 g/d DHA) eller daglig oral terapi med placebo. Etter 0, 4, 8 og 12 uker, på tvers av de 2 gruppene, vil tre spesifikke mål bli fulgt:
Mål 1. Sammenlign nivåer av EPA+DHA-avledede lipidmediatorer, og inflammatoriske cytokiner i blod og CVLU-væske.
Delmål 1a. Sammenlign inflammatorisk cytokin-genuttrykk av PMN-er i blod (nøytrofiler og monocytter).
Mål 2. Sammenlign PMN-aktivering (blod, CVLU-væske) og PMN-avledede proteasenivåer (CVLU-væske).
Mål 3. Sammenlign reduksjon i sårareal, kontroller for nøkkelfaktorer som er kjent for å påvirke tilheling, og bestemme forhold til lipidmediatorer, cytokiner og PMN-aktivering.
Delmål 3a. Sammenlign hyppigheten av CVLU-residiv og nivåer av studievariabler i blod mellom 2 undergrupper i EPA+DHA-gruppen med helbredede CVLUer (etter 3 ekstra måneder med EPA+DHA-behandling versus placeboterapi utover uke 12).
Delmål 3b. Sammenlign symptom på smerte til enhver tid og livskvalitet ved første og siste studiebesøk på tvers av de 2 gruppene og 2 undergruppene.
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
Ohio
-
Columbus, Ohio, Forente stater, 43210
- The Ohio State University College of Nursing
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Beskrivelse
Inklusjonskriterier:
Kvinner og menn ≥ 55 år med:
- En CVLU mellom ankel og kne som har vært tilstede i minst 4 uker, men ikke lenger enn 12 måneder, foreskrevet kompresjonsbehandling med 1-4 lags bandasjering;
- Ankel brachial trykkindeks (ABPI) mellom 0,7 og 1,2;
- Mål sårareal på 2-60 cm2 hvem kan
- Les og forstå engelsk eller spansk, og
- Gi samtykke.
Ekskluderingskriterier:
- Fiskeallergi;
- Kortikosteroider eller selektive cyklooksygenase (COX)-2-hemmere (f.eks. Celebrex); ikke-steroide antiinflammatoriske legemidler (NSAIDS) > 2 ganger/uke (unntak: aspirin 81 mg/dag);
- Autoimmune sykdommer;
- Kjemoterapi innen 6 måneder av uke 0;
- Diabetes hvis HbA1c > 12 % eller sår komplisert av cellulitt, eksponert sene eller ben.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: EPA+DHA Group
12 ukers daglig oral behandling med EPA+DHA (tre ugjennomsiktige myke geler for å gi et totalt daglig inntak på 1,87 g EPA + 1,0 g DHA)
|
EPA+DHA er de n-3 flerumettede fettsyrene som finnes i fiskeolje
Andre navn:
|
|
Placebo komparator: Placebo gruppe
12 uker med daglig oral behandling med placebo (tre ugjennomsiktige myke geler for å gi et totalt daglig inntak på 2,5 ml mineralolje)
|
placebo inneholder mineralolje
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
Tidsramme: 0, 4, 8 and 12 weeks
|
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.
|
0, 4, 8 and 12 weeks
|
|
Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE11
Tidsramme: 0, 4, 8 and 12 weeks
|
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.
|
0, 4, 8 and 12 weeks
|
|
Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE12
Tidsramme: 0, 4, 8 and 12 weeks
|
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.
|
0, 4, 8 and 12 weeks
|
|
Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE15
Tidsramme: 0, 4, 8 and 12 weeks
|
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.
|
0, 4, 8 and 12 weeks
|
|
Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE18
Tidsramme: 0, 4, 8 and 12 weeks
|
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.
|
0, 4, 8 and 12 weeks
|
|
Comparison of Intervention and Control Groups in IL-1β Levels (Log pg/mL)
Tidsramme: 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
|
|
Comparison of Intervention and Control Groups in IL-6 Levels (Log pg/mL)
Tidsramme: 0, 4, 8 and 12 weeks
|
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
|
|
1. Comparison of Intervention and Control Groups in TNF-α Levels (Log pg/mL)
Tidsramme: 0, 4, 8 and 12 weeks
|
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
|
|
Comparison of Intervention and Control Groups in IFN-γ Levels (Log pg/mL)
Tidsramme: 0, 4, 8 and 12 weeks
|
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
|
|
Intervention Effects on Polymorphonuclear Leukocyte (PMN) Activation (Log Cells/µL)
Tidsramme: 0, 4, 8 and 12 weeks
|
Reported values reflect PMN activation in plasma, expressed as log-transformed concentrations (cells/µL) at Weeks 4, 8, and 12.
|
0, 4, 8 and 12 weeks
|
|
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
|
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.
|
0, 4, 8 and 12 weeks
|
|
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
|
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.
|
0, 4, 8 and 12 weeks
|
|
Comparison of Intervention vs. Control Groups in the Percent Change in Wound Area Relative to Baseline
Tidsramme: 0, 4, 8 and 12 weeks
|
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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
Tidsramme: 0, 12 weeks
|
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.
|
0, 12 weeks
|
|
Venous Clinical Severity Score (VCSS)
Tidsramme: 0, 4, 8, 12 weeks
|
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.
|
0, 4, 8, 12 weeks
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Jodi C McDaniel, PhD, Ohio State University, College of Nursing
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2018H0261
- R01AG059981 (U.S. NIH-stipend/kontrakt)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .