Free Fatty Acid Effects In Type 2 Diabetes
Repositioning Omega-3 Fatty Acids For Treatment Of Glycaemia And Cardiometabolic Disease
Omega-3 fatty acids are natural fats found in foods such as oily fish and flaxseed. Omega-3 fatty acids have been found to have positive effects on cardiovascular health, but there is less evidence on if they can help manage blood glucose in individuals with both cardiovascular disease and type 2 diabetes.
This study will investigate whether the beneficial effects found in omega-3 fatty acids such as lowered blood glucose and reduced inflammation - both of which are important for managing type 2 diabetes and cardiovascular disease, can be beneficial for individuals with type 2 diabetes. As omega-3 fatty acids are already found naturally in food, and are already available as supplements, they could be a safe option to help manage these diseases.
The aim of this study is to investigate if omega-3 fatty acids can slow down the progression of type 2 diabetes and reduce the risk of cardiovascular disease in individuals with type 2 diabetes.
研究概览
地位
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习地点
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County Londonderry
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Coleraine、County Londonderry、英国、BT52 1SA
- School of Biomedical Sciences
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Individuals who are over 18 years of age with a BMI between 25-50 kg/m2, and who have been diagnosed with T2DM (>7.0 mmol/l fasting glucose) or pre-diabetes (impaired glucose tolerant 5.0-6.9mmol/l) and are either on no medication, are diet controlled or taking metformin. Participants may also have a history of cardiovascular disease.
Exclusion Criteria:
- Those who have severe or unstable cardiovascular disease
- Type 2 diabetics or prediabetics who are on an anti-diabetic medication (with the exception of metformin)
- Undergone recent major surgery or planned surgery during the study period
- Have implanted devices (such as pacemakers or defibrillators)
- Have an active infection
- Are involved in any other type of weight loss study/intervention
- Are pregnant/breastfeeding.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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安慰剂比较:安慰剂
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Receive placebo
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实验性的:Omega-3 Fatty Acid Supplementation (EPA/DHA)
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1500mg/day for 28 days
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实验性的:Omega-3 Fatty Acid Supplementation (ALA)
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1500mg/day for 28 days
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实验性的:Omega-3 Fatty Acid Supplementation (EPA/DHA) and Semaglutide
Semaglutide is being used for comparison purposes only
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1500mg/day for 28 days
0.25mg weekly for four weeks
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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To evaluate the change in fasting glucose from baseline after 28 days of treatment, compared to each treatment group and placebo.
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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The change in insulin compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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The change in HbA1c compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Glucose tolerance measurements during OGTT compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Area under the curve measurements during OGTT compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Plasma gut hormone concentrations (GLP-1, GIP, PYY, ghrelin, CCK and glucagon) compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Full lipid profile (cardiovascular risk markers) compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Inflammatory and cardiovascular markers compared to placebo administration
大体时间:From baseline to 28 days of treatment
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Biomarkers include inflammatory markers (C-reactive protein [CRP], pro- and anti-inflammatory cytokines) and cardiovascular risk markers
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From baseline to 28 days of treatment
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Liver function tests (ALT and AST) compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Body mass index (BMI) compared to placebo administration
大体时间:From baseline to 28 days of treatment
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Weight (kg) and height (m) will be combined to report BMI in kg/m^2
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From baseline to 28 days of treatment
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Waist-to-hip circumference compared to placebo administration
大体时间:From baseline to 28 days of treatment
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Waist circumference (in cm between the lower rib and iliac crest) and hip circumference (in cm at the widest part of the hips/buttocks) will be combined to calculate waist-to-hip circumference
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From baseline to 28 days of treatment
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Blood pressure compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) index compared to placebo administration
大体时间:From baseline to 28 days of treatment
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Insulin resistance will be measured by calculating HOMA-IR using the formula: HOMA-IR = fasting plasma glucose (mg/dL) x fasting plasma insulin/405.
Higher values indicate greater insulin resistance.
This is a derived continuous index with no fixed minimum or maximum value.
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From baseline to 28 days of treatment
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Change in Omega-3 Index (EPA and DHA as a percentage of total fatty acids) compared to placebo administration
大体时间:From baseline to 28 days of treatment
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From baseline to 28 days of treatment
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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