NL-OMON56896尚未招募不适用
The effect of algae oil supplements on functional immune response and bioavailability of lipids in blood, a pilot study - ALG study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 12
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Apparently healthy men and women;
- •- Age >= 50 years
- •- Body mass index (BMI) >=18.5 and <=30 kg/m2;
- •- Having veins suitable for blood sampling via a catheter (judged by study
- •nurse/ medical doctor);
- •- Willing to refrain from fish, fish oil, and products with added omega-3
- •starting from one 2 weeks prior to first postprandial test day.
- •- Willing to keep a stable dietary pattern throughout the study
排除标准
- •- Having a disease that may interfere with the outcomes of this study, such as
- •a known metabolic, gastrointestinal, inflammatory or chronic disease (such as
- •anaemia, diabetes, hepatitis, cardiovascular disease), as judged by the medical
- •investigator;
- •- Having a history of medical or surgical events that may significantly affect
- •the study outcome, including: Inflammatory bowel disease, hepatitis,
- •pancreatitis, ulcers, gastrointestinal or rectal bleeding; major
- •gastrointestinal tract surgery such as gastrectomy, gastroenterostomy, or bowel
- •resection; known or suspected gastrointestinal disorders, colon or GI tract
- •- Use of medication that may interfere with the study outcomes, including
- •gastric acid in-hibitors or laxatives, as judged by the medical supervisor.
- •- Anaemia (Haemoglobin (Hb) values <7.5 mmol/L for women and <8.5 mmol/L for
- •men), as assessed by finger prick blood during screening visit;
- •- Having swallowing problems with capsules;
- •- Allergic for fish or shellfish;
- •- Recent blood donation (<1 month prior to test day 1 of the study) or not
- •willing to stop donation during and 1 month after the study;
- •- Average alcohol intake >21 (women) or >28 (men) glasses of alcoholic
- •beverages per week;
- •- Reported weight loss or weight gain of more than 3 kg in the month prior to
- •pre-study screening, or intention to lose weight during the study period;
- •- Reported to follow or having planned a slimming or medically prescribed diet;
- •- Use of drugs;
- •- Current smokers, or stopped smoking in the last 3 months before study start;
- •- Insufficient proficiency in Dutch to understand information brochure and
- •questionnaires;
- •- Participation in any clinical trial including blood sampling and/or
- •administration of sub-stances up to 30 days before test day 1 of this study and
- •during the study period;
- •- Being an employee of the department Food, Health & Consumer Research or Food
- •Quality and Design of Wageningen Food & Biobased Research.
研究者
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