ACTRN12610000285055尚未招募未知
A 12-week randomised, parallel dietary intervention to compare the effects of consuming 30g or 60g of nuts per day, or no nuts (control) on biomarkers of chronic disease, including blood lipids, inflammation, endothelial function, and body composition in overweight and obese individuals.
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 65 Years（—）
- 性别
- All
入选标准
- •The inclusion criteria are males and females aged between 18 and 65 years with a Body Mass Index (BMI) greater than or equal to 25 [weight (kg) / height (m2)]
排除标准
- •The exclusion criteria are smokers. Pregnant or breastfeeding women. People who have asthma. People who are on weight loss programmes. People with food allergies or food aversions to nuts. People who have inflammatory diseases such as Crohn's or Celiac disease. People who have familial or secondary hyperlipidaemia or major chronic diseases such as cancer, heart disease or diabetes. People who are taking medication known to affect inflammatory markers, e.g. aspirin, ibuprofen, naproxen, glucocorticoids, etc.
研究者
相似试验
尚未招募
不适用
Improving the adherence to action plans in patients with chronic obstructive pulmonary diseaseChronic Obstructive Pulmonary Disease (COPD)Respiratory - Chronic obstructive pulmonary diseasePublic Health - Health service researchACTRN12612000269831Royal Prince Alfred Hospital90
进行中（未招募）
2 期
Study of efficacy and safety of SAF312 eye drops in subjects with post-operative corneal induced chronic pain (CICP)JPRN-jRCT2011220008Yamada Hiroyuki15
已完成
不适用
Psychological treatments of post-traumatic stress disorderPost-traumatic stress disorder (PTSD)Mental and Behavioural DisordersStress disordersISRCTN48524925King's College London (UK)120
进行中（未招募）
不适用
A 12-week treatment, randomized, double-blind, parallel group, multicenter study to evaluate the efficacy of the valsartan/simvastatin combinations 160/20mg up titrated to 320/20mg versus 160/40mg up titrated to 320/40mg in patients with both essential hypertension and hypercholesterolemiaEssential hypertension and hypercholesterolemiaEUCTR2005-002382-36-DEovartis Pharma Services AG796
进行中（未招募）
不适用
A 12-week treatment, randomized, double-blind, parallel group, multicenter study to evaluate the efficacy of the valsartan/simvastatin combinations 160/20mg up titrated to 320/20mg versus 160/40mg up titrated to 320/40mg in patients with both essential hypertension and hypercholesterolemiaEUCTR2005-002382-36-SEovartis Pharma Services AG796