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临床试验/NCT03746093
NCT03746093Unknown不适用

Effects of Non-alcoholic Beer in Patients With Type 2 Diabetes: A Randomized Controlled Trial

Universidade do Porto2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年11月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
30
试验地点
2
主要终点
Changes in fasting capillary blood glucose from baseline to visit 2 and 3

研究概览

简要总结

The aim of the study is to investigate the effects of non-alcoholic beer in patients with type 2 diabetes. Subjects will be divided into two groups: the control group, where participants will be consuming a bottle of water (330ml) every day for 12 weeks, and the intervention group, where participants will be consuming a bottle of non-alcoholic beer (330ml) for the same period.

详细描述

This is a parallel, controlled randomized trial. The study will compare the effect of non-alcoholic beer consumption with water, in patients with type 2 diabetes.

All patients from both groups will receive a personalized nutritional intervention and will be followed throughout the study by a certified nutritionist.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women diagnosed with type 2 diabetes mellitus, according to the American Diabetes Association criteria;
  • Ages 40-80 years;
  • Non-smoker;
  • Willing and able to provide written informed consent.

排除标准

  • Changes in oral glycaemic-control medications in the last 3 months;
  • Subjects with HbA1c levels under 6.4% or above 10%;
  • Subjects under insulinotherapy;
  • Subjects with triglycerides levels above 4.52 nmol/L(400 mg/dL);
  • Intake of antibiotics in the last 12 weeks;
  • Subjects not willing to avoid drinking beer during the study;
  • Subjects with a diagnosis of any digestive disease including functional bowel disorders such as IBS;
  • Pregnant women or women planning to become pregnant during the study.

研究组 & 干预措施

Non-alcoholic beer

Experimental

Participants will consume non-alcoholic beer (330 ml) every day for 12 weeks.

干预措施: Non-alcoholic beer (Dietary Supplement)

Control Group

Placebo Comparator

Participants will consume a bottle of water (330 ml) every day for 12 weeks.

干预措施: Water (Dietary Supplement)

结局指标

主要结局

Changes in fasting capillary blood glucose from baseline to visit 2 and 3

时间窗: at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period)

Changes in fasting insulin levels from baseline to visit 2 and 3

时间窗: at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period)

Changes in HOMA-B from baseline to visit 2 and 3

时间窗: at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period)

Changes in HbA1c levels from baseline to visit 2 and 3

时间窗: at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period)

Changes in HOMA-IR from baseline to visit 2 and 3

时间窗: at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period)

次要结局

  • Changes in body mass index from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))
  • Changes in fasting serum triglycerides from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))
  • Changes in total body fat mass from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))
  • Changes in fasting serum low-density lipoprotein (LDL) cholesterol from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))
  • Changes in fasting serum total cholesterol from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))
  • Changes in intestinal microbiota from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))
  • Changes in fasting serum high-density lipoprotein (HDL) cholesterol from baseline to visit 2 and 3(at visit 1 (after 1-week run-in period), visit 2 (after 6-week intake period), visit 3 (after 12-week intake period))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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