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- Ensaio Clínico NCT03576989
Impacto da terapia oral com ácidos graxos ômega-3 na cicatrização de úlceras venosas crônicas em adultos mais velhos
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
A patogênese da CVLU envolve altos números de leucócitos polimorfonucleares ativados (PMN) que estão associados à inflamação persistente no leito da ferida. A pesquisa proposta é testar a eficácia de uma intervenção nutricional oral contendo os componentes bioativos do óleo de peixe (ácido eicosapentaenóico - EPA + ácido docosahexaenóico - DHA) para amenizar a atividade de PMN e promover a cicatrização. O estudo planeja incluir 248 adultos sucessivamente elegíveis ≥ 55 anos de idade com CVLUs que continuam a receber tratamento padrão em duas clínicas de feridas ambulatoriais universitárias. Os participantes serão randomizados em 2 grupos: 12 semanas de terapia oral diária com EPA+DHA (1,87 g/d de EPA + 1,0 g/d de DHA) ou terapia oral diária com placebo. Nas 0, 4, 8 e 12 semanas, nos 2 grupos, três objetivos específicos serão perseguidos:
Objetivo 1. Comparar os níveis de mediadores lipídicos derivados de EPA+DHA e citocinas inflamatórias no sangue e fluido CVLU.
Subobjetivo 1a. Comparar a expressão de genes de citocinas inflamatórias por PMNs no sangue (neutrófilos e monócitos).
Objetivo 2. Comparar a ativação de PMN (sangue, fluido CVLU) e os níveis de protease derivada de PMN (fluido CVLU).
Objetivo 3. Comparar a redução na área da ferida, controlando os principais fatores conhecidos por afetar a cicatrização e determinar as relações com mediadores lipídicos, citocinas e ativação de PMN.
Subobjetivo 3a. Compare a frequência de recorrência de CVLU e os níveis de variáveis de estudo no sangue entre 2 subgrupos dentro do grupo EPA+DHA com CVLUs curados (após 3 meses adicionais de terapia com EPA+DHA versus terapia com placebo após o ponto de tempo da Semana 12).
Subobjetivo 3b. Compare o sintoma de dor em todos os momentos e a qualidade de vida na primeira e na última visita do estudo nos 2 grupos e 2 subgrupos.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
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Ohio
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Columbus, Ohio, Estados Unidos, 43210
- The Ohio State University College of Nursing
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Descrição
Critério de inclusão:
Mulheres e homens ≥ 55 anos de idade com:
- Uma CVLU entre o tornozelo e o joelho presente há pelo menos 4 semanas, mas não mais que 12 meses, prescreveu terapia de compressão com bandagem de 1-4 camadas;
- Índice de pressão tornozelo-braquial (IPB) entre 0,7 e 1,2;
- Alvo área da ferida de 2-60 cm2 que pode
- Ler e compreender inglês ou espanhol, e
- Fornecer consentimento.
Critério de exclusão:
- Alergia a peixe;
- Corticosteróides ou inibidores seletivos da ciclooxigenase (COX)-2 (por exemplo, Celebrex); anti-inflamatórios não esteroidais (AINEs) > 2x/semana (exceção: aspirina 81 mg/dia);
- Doenças autoimunes;
- Quimioterapia dentro de 6 meses da Semana 0;
- Diabetes se HbA1c > 12% ou úlcera complicada por celulite, tendão ou osso exposto.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Triplo
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Grupo EPA+DHA
12 semanas de terapia oral diária com EPA+DHA (três cápsulas moles opacas para fornecer uma ingestão diária total de 1,87 g de EPA + 1,0 g de DHA)
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EPA+DHA são os ácidos graxos poliinsaturados n-3 contidos no óleo de peixe
Outros nomes:
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Comparador de Placebo: Grupo Placebo
12 semanas de terapia oral diária com placebo (três cápsulas moles opacas para fornecer uma ingestão diária total de 2,5 mL de óleo mineral)
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placebo contém óleo mineral
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
Prazo: 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)
Prazo: 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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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Jodi C McDaniel, PhD, Ohio State University, College of Nursing
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Doenças de pele
- Úlcera de pele
- Doenças da Pele e do Tecido Conjuntivo
- Úlcera de perna
- Ferimentos e Lesões
- Produtos químicos orgânicos
- Ácidos graxos
- Lipídios
- Hidrocarbonetos
- Eicosanóides
- Ácidos graxos, insaturados
- Óleos
- Gorduras alimentares
- Gorduras
- Ácidos graxos, ômega-3
- Gorduras alimentares, insaturadas
- Petrolatum
- Óleo mineral
- Ácido eicosapentaenóico
- Ácidos docosahexaenóicos
- Óleos de peixe
Outros números de identificação do estudo
- 2018H0261
- R01AG059981 (Concessão/Contrato do NIH dos EUA)
Plano para dados de participantes individuais (IPD)
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