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- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT01072864
Effects of California Walnuts on Vascular Function in Postmenopausal Women
To determine the potential acute cardiovascular benefits of California Walnuts in postmenopausal women of ages 55-70.
Primary outcome measures:
- Vascular function
- Platelet reactivity
We hypothesize that the consumption of California walnuts will improve vascular function and platelet reactivity.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Epidemiological studies have shown that consumption of high amounts of plant foods, such as nuts, fruits and vegetables, appears to be protective against chronic diseases including heart disease, stroke, diabetes mellitus and metabolic syndrome. In recent years, numerous studies indicate that consumption of walnuts mainly containing α-linolenic acid (ALA), L-arginine and polyphenols beneficially alters vascular function and reduces inflammatory biomarkers. Recent studies have reported that consumption of walnuts is associated with beneficial effects in prevention of chronic diseases by favorably altering human serum profiles (i.e. decrease in LDL cholesterol and triglycerides and increase in HDL cholesterol and apolipoprotein A1) which are closely involved in the development of cardiovascular disease (CVD). In addition, recent reports by Dr. Ros and his colleagues indicate that addition of walnuts to a high-fat meal can improve endothelial function. This favorable influence on vasoactivity has been attributed to the antioxidant and anti-inflammatory properties of components of walnuts.
Due to their age and menopausal status, postmenopausal women in particular, are at a greater risk population for developing CVD. Males tend to show greater rates of CVD than pre-menopausal women, while women following menopause show an increase in the rates of CVD. This increase is associated with endothelial dysfunction and decreased vasodilation which are apparently expressed after menopause and become worse with age. In this study, we will define the effects of consuming California walnuts on vascular health.
We hypothesize that consumption of California walnuts, which are particularly rich in ALA, L-arginine and polyphenols, will improve endothelial function and platelet reactivity in an at-risk population of postmenopausal women 50-70 years of age.
Tipo de estudo
Inscrição (Real)
Estágio
- Fase 1
Contactos e Locais
Locais de estudo
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California
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Davis, California, Estados Unidos, 95616
- Ragle Human Nutrition Research Center
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- 50 to 70 years of age
- Lack of menses in the last year and FSH 23-116.3 mlU/mL
- Subject is willing and able to comply with the study protocols.
- Subject is willing to consume up to 40 g of California walnuts.
- BMI 18.5-34.9 kg/m2
- Weight ≥ 110 pounds
Exclusion Criteria:
- BMI ≥ 35 kg/m2
- Weight <110 pounds
- Diabetes
- Taking anticoagulation medication including NSAIDs
- Blood pressure ≥ 160/90 mm Hg
- PFA-100 readings 10 % outside of normal reference range (normal reference range for ADP-Collagen: 71-118 sec; Epinephrine-Collagen: 94-193 sec).
- Renal or liver disease
- Heart disease, which includes cardiovascular events and Stroke
- Cushing's syndrome
- Chronic/routine high intensity exercise
- Inability to properly place or wear the PAT probes or abnormal measurements on pre-screening PAT
- Abnormal Liver, CBC or CMP (laboratory values outside the reference range) if determined to be clinically significant.
- History of cancer
- History of psychiatric disorders i.e. schizophrenia or bi-polar or depression treated with antidepressants within the last 1 year.
- Use of MAOI inhibitor within the last 1 year (e.g. phenelzine (Nardil), tranylcypromine (Parnate), etc)
- Malabsorption
- Anxiety medications
- Routine use of prescription drugs or over-the counter medications, which may potentially modulate the outcome of this study; including antibiotics, aspirin and aspirin-containing formulations, COX-2 inhibitors, antihistamines, corticosteroids, ACE-inhibitors, and beta-blockers.
- Asthma (can be worsened by mild to moderate food allergies).
- Indications of substance or alcohol abuse within the last 3 years
- Use of multivitamin/mineral supplements
- Use of herbal or plant-based supplements; omega-3 fatty acids, and fish oils in the past 3-6 months.
- Nut allergies
- Soy-derived supplements
- Soy/soy products consumption > 2 servings/week
- Hormone replacement therapy
- Alcohol consumption > 1 drink/day (i.e. 1 bottle of beer, ½ glass of wine, and 1 shot of hard liquor)
- Fruit consumption ≥ 3 cups (6 servings)/day
- Vegetable consumption ≥ 4 cups (8 servings)/day
- Grain consumption ≥ 8 oz/day
- Meat and Beans ≥ 7 oz/day
- Fatty Fish ≥ 3 times/week
- Milk ≥ 5 cups/day
- Oil ≥ 8 tsp/day
- Coffee/tea ≥ 3 cups/day
- Dark chocolate ≥ 3 oz/day
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Ciência básica
- Alocação: Randomizado
- Modelo Intervencional: Atribuição cruzada
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: 5 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
|
Experimental: 20 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
|
Experimental: 30 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
|
Experimental: 40 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
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Peripheral Arterial Tonometry (PAT)
Prazo: 2 and 4 hours
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2 and 4 hours
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Robert M. Hackman, PhD, University of California, Davis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
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 (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
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
Outros números de identificação do estudo
- 200917508-1
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
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