- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT03576989
Impatto della terapia orale con acidi grassi omega-3 sulla guarigione delle ulcere venose croniche delle gambe negli anziani
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
La patogenesi della CVLU coinvolge un numero elevato di leucociti polimorfonucleati attivati (PMN) che sono associati a un'infiammazione persistente nel letto della ferita. La ricerca proposta è quella di testare l'efficacia di un intervento nutritivo orale contenente i componenti bioattivi dell'olio di pesce (acido eicosapentaenoico - EPA + acido docosaesaenoico - DHA) per attenuare l'attività dei PMN e promuovere la guarigione. Lo studio prevede di includere 248 adulti ammissibili consecutivi di età ≥ 55 anni con CVLU che continuano a ricevere cure standard presso due cliniche universitarie ambulatoriali per le ferite. I partecipanti saranno randomizzati in 2 gruppi: 12 settimane di terapia orale quotidiana con EPA+DHA (1,87 g/giorno di EPA + 1,0 g/giorno di DHA) o terapia orale quotidiana con placebo. A 0, 4, 8 e 12 settimane, nei 2 gruppi, verranno perseguiti tre obiettivi specifici:
Obiettivo 1. Confrontare i livelli di mediatori lipidici derivati da EPA+DHA e di citochine infiammatorie nel sangue e nel fluido CVLU.
Sottoobiettivo 1a. Confronta l'espressione genica delle citochine infiammatorie da parte dei PMN nel sangue (neutrofili e monociti).
Obiettivo 2. Confrontare l'attivazione dei PMN (sangue, fluido CVLU) ei livelli di proteasi derivati dai PMN (fluido CVLU).
Obiettivo 3. Confrontare la riduzione dell'area della ferita, controllando i fattori chiave noti per influenzare la guarigione e determinare le relazioni con i mediatori lipidici, le citochine e l'attivazione dei PMN.
Sottoobiettivo 3a. Confrontare la frequenza di recidiva di CVLU e i livelli delle variabili dello studio nel sangue tra 2 sottogruppi all'interno del gruppo EPA+DHA con CVLU guariti (dopo 3 mesi aggiuntivi di terapia con EPA+DHA rispetto alla terapia con placebo oltre il punto temporale della settimana 12).
Sottoobiettivo 3b. Confrontare il sintomo del dolore in tutti i momenti e la qualità della vita alla prima e all'ultima visita dello studio nei 2 gruppi e nei 2 sottogruppi.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Ohio
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Columbus, Ohio, Stati Uniti, 43210
- The Ohio State University College of Nursing
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Descrizione
Criterio di inclusione:
Donne e uomini di età ≥ 55 anni con:
- Un CVLU tra caviglia e ginocchio presente da almeno 4 settimane, ma non più di 12 mesi, prescritta terapia compressiva con bendaggio a 1-4 strati;
- Indice pressorio caviglia brachiale (ABPI) compreso tra 0,7 e 1,2;
- Target area della ferita di 2-60 cm2 che può
- Leggere e comprendere l'inglese o lo spagnolo e
- Fornire il consenso.
Criteri di esclusione:
- Allergia al pesce;
- Corticosteroidi o inibitori selettivi della cicloossigenasi (COX)-2 (ad es. Celebrex); farmaci antinfiammatori non steroidei (FANS) > 2 volte/settimana (eccezione: aspirina 81 mg/die);
- Malattie autoimmuni;
- Chemioterapia entro 6 mesi dalla settimana 0;
- Diabete se HbA1c > 12% o ulcera complicata da cellulite, tendine o ossa esposte.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Gruppo EPA+DHA
12 settimane di terapia orale giornaliera con EPA+DHA (tre softgel opache per fornire un apporto giornaliero totale di 1,87 g di EPA + 1,0 g di DHA)
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EPA+DHA sono gli acidi grassi polinsaturi n-3 contenuti nell'olio di pesce
Altri nomi:
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Comparatore placebo: Gruppo placebo
12 settimane di terapia orale giornaliera con placebo (tre capsule molli opache per fornire un'assunzione giornaliera totale di 2,5 ml di olio minerale)
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il placebo contiene olio minerale
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
Lasso di tempo: 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.
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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
Lasso di tempo: 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.
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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
Lasso di tempo: 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
Lasso di tempo: 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.
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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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
|
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1. Comparison of Intervention and Control Groups in TNF-α Levels (Log pg/mL)
Lasso di tempo: 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
|
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Comparison of Intervention and Control Groups in IFN-γ Levels (Log pg/mL)
Lasso di tempo: 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
|
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) Activation (Log Cells/µL)
Lasso di tempo: 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.
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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
Lasso di tempo: 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.
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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
Lasso di tempo: 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
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
Lasso di tempo: 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.
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0, 12 weeks
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Venous Clinical Severity Score (VCSS)
Lasso di tempo: 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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Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Jodi C McDaniel, PhD, Ohio State University, College of Nursing
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie della pelle
- Ulcera della pelle
- Malattie della pelle e del tessuto connettivo
- Ulcera alla gamba
- Ferite e lesioni
- Prodotti chimici organici
- Acidi grassi
- Lipidi
- Idrocarburi
- Eicosanoidi
- Acidi grassi, insaturi
- Oli
- Grassi dietetici
- Grassi
- Acidi grassi, Omega-3
- Grassi dietetici, insaturi
- Petrolatum
- Olio minerale
- Acido eicosapentaenoico
- Acidi docosaesaenoici
- Oli di pesce
Altri numeri di identificazione dello studio
- 2018H0261
- R01AG059981 (Sovvenzione/contratto NIH degli Stati Uniti)
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .