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- Ensayo clínico NCT03576989
Impacto de la terapia oral con ácidos grasos omega-3 en la cicatrización de las úlceras venosas crónicas de las piernas en adultos mayores
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
La patogenia de CVLU involucra un alto número de leucocitos polimorfonucleares activados (PMN) que están asociados con inflamación persistente en el lecho de la herida. La investigación propuesta es probar la eficacia de una intervención nutricional oral que contiene los componentes bioactivos del aceite de pescado (ácido eicosapentaenoico - EPA + ácido docosahexaenoico - DHA) para aliviar la actividad de PMN y promover la curación. El estudio planea incluir a 248 adultos elegibles sucesivos ≥ 55 años de edad con CVLU que continúan recibiendo atención estándar en dos clínicas universitarias ambulatorias de heridas. Los participantes serán asignados aleatoriamente a 2 grupos: 12 semanas de terapia oral diaria con EPA+DHA (1,87 g/día de EPA + 1,0 g/día de DHA) o terapia oral diaria con placebo. A las 0, 4, 8 y 12 semanas, en los 2 grupos, se perseguirán tres objetivos específicos:
Objetivo 1. Comparar los niveles de mediadores lipídicos derivados de EPA+DHA y citoquinas inflamatorias en sangre y líquido CVLU.
Subaim 1a. Comparar la expresión génica de citoquinas inflamatorias por PMN en sangre (neutrófilos y monocitos).
Objetivo 2. Comparar la activación de PMN (sangre, líquido CVLU) y los niveles de proteasa derivados de PMN (líquido CVLU).
Objetivo 3. Comparar la reducción del área de la herida, controlar los factores clave que se sabe que afectan la cicatrización y determinar las relaciones con los mediadores de lípidos, las citocinas y la activación de PMN.
Subaim 3a. Compare la frecuencia de recurrencia de CVLU y los niveles de las variables del estudio en sangre entre 2 subgrupos dentro del grupo de EPA+DHA con CVLU curadas (después de 3 meses adicionales de terapia con EPA+DHA versus terapia con placebo más allá del punto de tiempo de la semana 12).
Subaim 3b. Compare el síntoma de dolor en todos los puntos temporales y la calidad de vida en la primera y última visita del estudio en los 2 grupos y 2 subgrupos.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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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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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Descripción
Criterios de inclusión:
Mujeres y hombres ≥ 55 años con:
- Un CVLU entre el tobillo y la rodilla que ha estado presente durante al menos 4 semanas, pero no más de 12 meses, prescribió terapia de compresión con vendaje de 1 a 4 capas;
- Índice de presión brazo-tobillo (ABPI) entre 0,7 y 1,2;
- Área de herida objetivo de 2-60 cm2 que puede
- Leer y entender inglés o español, y
- Dar consentimiento.
Criterio de exclusión:
- alergia al pescado;
- Corticosteroides o inhibidores selectivos de la ciclooxigenasa (COX)-2 (p. ej., Celebrex); fármacos antiinflamatorios no esteroideos (AINE) > 2x/semana (excepción: aspirina 81 mg/día);
- Enfermedades autoinmunes;
- Quimioterapia dentro de los 6 meses de la Semana 0;
- Diabetes si HbA1c > 12% o úlcera complicada con celulitis, tendón o hueso expuesto.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Grupo EPA+DHA
12 semanas de terapia oral diaria con EPA+DHA (tres cápsulas blandas opacas para proporcionar una ingesta diaria total de 1,87 g de EPA + 1,0 g de DHA)
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EPA+DHA son los ácidos grasos poliinsaturados n-3 contenidos en el aceite de pescado
Otros nombres:
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Comparador de placebos: Grupo placebo
12 semanas de terapia oral diaria con placebo (tres cápsulas blandas opacas para proporcionar una ingesta diaria total de 2,5 ml de aceite mineral)
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el placebo contiene aceite mineral
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
Periodo de tiempo: 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)
Periodo de tiempo: 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
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades de la piel
- Úlcera de la piel
- Enfermedades de la piel y del tejido conectivo
- Úlcera en la pierna
- Heridas y Lesiones
- Químicos orgánicos
- Ácidos grasos
- Lípidos
- Hidrocarburos
- Eicosanoides
- Ácidos grasos, insaturados
- Aceites
- Grasas dietéticas
- Grasas
- Ácidos grasos, omega-3
- Grasas dietéticas, insaturadas
- Gasolatón
- Aceite mineral
- Ácido eicosapentaenoico
- Ácidos docoshexaenoicos
- Aceites de pescado
Otros números de identificación del estudio
- 2018H0261
- R01AG059981 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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