Ranasinghe Priyanga, Galappaththy Priyadarshani, Constantine Godwin Roger, Jayawardena Ranil, Weeratunga Hasitha Dhananjaya, Premakumara Sirimal, Katulanda Prasad
Department of Pharmacology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
Department of Clinical Medicine, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
Trials. 2017 Sep 29;18(1):446. doi: 10.1186/s13063-017-2192-0.
Previous studies have explored the anti-diabetic effects of Cinnamomum cassia extract in vivo and in vitro. However, there are no studies at present exploring the effects of the indigenous species of Sri Lankan cinnamon (Cinnamomum zeylanicum) in patients with diabetes mellitus. The present study aims to evaluate the potential effects of Cinnamomum zeylanicum extract as a pharmaceutical agent in patients with type-2 diabetes mellitus.
METHODS/DESIGN: The study will be conducted as a randomized, double-blind, placebo-controlled clinical trial for a period of 4 months at the Medical Clinic, University Medical Unit, National Hospital of Sri Lanka. A total of 210 subjects with diabetes, in three equal groups, will be recruited for the study. The patients will be randomized in a 1:1:1 ratio according to the method of block randomization and the subjects will be randomly and equally assigned into two test groups (n = 70 each) and one placebo group (n = 70). The population will be stratified at randomization based on age, gender and disease severity. The treatment drug is a capsule containing Cinnamomum zeylanicum extract as the active ingredient and the placebo capsule will contain lactose monohydrate. Two doses of Cinnamomum zeylanicum extracts (250 mg and 500 mg of the cinnamon extract) will be used. The study drugs will be double blinded to both investigators and participants. The visits and the evaluations will be done as follows: screening (visit 0), 1 month (visit 1), 2 months (visit 2), 3 months (visit 3) and 4 months (visit 4). The following primary outcome measures will be evaluated: glycosylated hemoglobin (HbAc), fasting plasma glucose (FPG) and serum insulin. Secondary outcome measures include: Body Mass Index (BMI) and other anthropometric parameters, blood pressure, total cholesterol, low-density lipoprotein cholesterol (LDL), high-density lipoprotein cholesterol (HDL) and triglycerides (TAG). Data will be analyzed using SPSS version 14.
We describe the protocol for a clinical trial design evaluating the effects of Cinnamomum zeylanicum (Ceylon cinnamon) in patients with type-2 diabetes mellitus. The result of the present study, positive or negative, should provide a step change in the evidence guiding current and future policies regarding the use of cinnamon dietary supplementation in patients with diabetes.
Sri Lanka Clinical Trials Registry (SLCTR), identifier: SLCTR/2017/010 ( http://slctr.lk/trials/714 ). Registered on 5 April 2017; study protocol version 3.1 21 March 2017.
此前的研究已在体内和体外探究了肉桂提取物的抗糖尿病作用。然而,目前尚无研究探讨斯里兰卡土生土长的肉桂品种(锡兰肉桂)对糖尿病患者的影响。本研究旨在评估锡兰肉桂提取物作为一种药物制剂对2型糖尿病患者的潜在作用。
方法/设计:本研究将在斯里兰卡国家医院大学医疗单元的医务室进行一项为期4个月的随机、双盲、安慰剂对照临床试验。总共210名糖尿病患者将被招募并平均分为三组参与研究。患者将按照区组随机化方法以1:1:1的比例随机分组,受试者将被随机且平均地分配到两个试验组(每组n = 70)和一个安慰剂组(n = 70)。研究对象将在随机分组时根据年龄、性别和疾病严重程度进行分层。治疗药物是一种以锡兰肉桂提取物为活性成分的胶囊,安慰剂胶囊将含有一水乳糖。将使用两种剂量的锡兰肉桂提取物(250毫克和500毫克肉桂提取物)。研究药物对研究者和参与者均为双盲。访视和评估将按以下方式进行:筛查(访视0)、1个月(访视1)、2个月(访视2)、3个月(访视3)和4个月(访视4)。将评估以下主要结局指标:糖化血红蛋白(HbAc)、空腹血糖(FPG)和血清胰岛素。次要结局指标包括:体重指数(BMI)和其他人体测量参数、血压、总胆固醇、低密度脂蛋白胆固醇(LDL)、高密度脂蛋白胆固醇(HDL)和甘油三酯(TAG)。数据将使用SPSS 14版软件进行分析。
我们描述了一项评估锡兰肉桂对2型糖尿病患者影响的临床试验设计方案。本研究的结果,无论阳性或阴性,都应为指导当前及未来关于糖尿病患者使用肉桂膳食补充剂的政策的证据带来一个阶段性的变化。
斯里兰卡临床试验注册中心(SLCTR),标识符:SLCTR/2017/010(http://slctr.lk/trials/714)。于2017年4月5日注册;研究方案版本3.1,2017年3月21日。