ISRCTN03372660已完成2 期
Effect of olive oil enriched in oleanolic acid on the incidence of type 2 diabetes mellitus in patients with pre-diabetes: a multicentre randomised double-blind controlled trial
Andalusian Regional Ministry of Health (Consejería de Salud de la Junta de Andalucía) (Spain)0 个研究点目标入组 176 人开始时间: 2009年11月3日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 176
研究概览
简要总结
2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/31364228 (added 01/08/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Current information as of 09/11/09:
- •1. Men or women with an age range between 30 and 80 years
- •2. Body mass index = 25 kg/m^2 and < 40 kg/m^2
- •3. Acceptance to participate in the study and signed the corresponding informed consent
- •Initial information at time of registration:
- •1. Men or women with an age range between 30 and 80 years
- •2. Body mass index = 25 kg/m^2
- •3. Acceptance to participate in the study and signed the corresponding informed consent
排除标准
- •Current information as of 09/11/09:
- •1. Diabetes at the time of admission to the study:
- •1.1. Glycaemia baseline = 126 mg/dl or glycaemia 2 hours after the oral overload
- •1.2. 75 g of glucose = 200 mg/dl
- •1.3. Diabetes confirmed by a physician and confirmed by other clinical data
- •1.4. In antidiabetic treatment (oral and/or insulin)
- •2. Alcohol dependence syndrome or any other addiction
- •3. Physical, mental or intellectual limitation to take part in a study of dietary intervention
- •4. Difficulty or lack of predisposition to change food habits
- •5. Drugs or medical conditions that interfere with the diagnosis of diabetes:
- •5.1. Beta-blockers
- •5.2. Systemic glucocorticoids
- •5.3. Selective inhibitors of the reuptake of serotonin at doses indicated for weight reduction
- •5.4. Other drugs for weight reduction (orlistat and sibutramine)
- •5.5. Thyroid Disease suboptimal treatment
- •5.6. Other endocrine diseases (such as Cushing's disease, acromegaly)
- •5.7. Fasting triglycerides > 600 mg/dl despite treatment
- •6. Conditions or circumstances which may affect the conduct of the trial:
- •6.1. Inability to communicate with the researchers conducting the intervention
- •6.2. Not willing to accept the treatment assigned by randomisation
- •6.3. Participation in another project that could interfere with this project
- •6.4. Loss of weight for any reason superior to 10 % in the last three months, except postpartum
- •6.5. Inability to walk 400 meters in 10 minutes without stopping
- •7. Cancer in the last 5 years that needed treatment, unless the prognosis is good
- •8. Systolic blood pressure = 180 mmHg and/or diastolic blood pressure = 110 mmHg
- •9. Pregnant women of childbearing age, if:
- •9.1. Currently pregnant or within 3 months postpartum
- •9.2. Lactating
- •9.3. Pregnancy planned during the study period
- •Initial information at time of registration
- •1. Diabetes at the time of admission to the study:
- •1.1. Glycaemia baseline = 126 mg/dl or glycaemia 2 hours after the oral overload
- •1.2. 75 g of glucose = 200 mg/dl
- •1.3. Diabetes confirmed by a physician and confirmed by other clinical data
- •1.4. In antidiabetic treatment (oral and/or insulin)
- •2. Alcohol dependence syndrome or any other addiction
- •3. Physical, mental or intellectual limitation to take part in a study of dietary intervention
- •4. Difficulty or lack of predisposition to change food habits
- •5. Drugs or medical conditions that interfere with the diagnosis of diabetes:
- •5.1. Thiazide diuretics
- •5.2. Beta-blockers
- •5.3. Systemic glucocorticoids
- •5.4. Selective inhibitors of the reuptake of serotonin at doses indicated for weight reduction
- •5.5. Other drugs for weight reduction (orlistat and sibutramine)
- •5.6. Thyroid Disease suboptimal treatment
- •5.7. Other endocrine diseases (such as Cushing's disease, acromegaly)
研究者
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