研究疾病:
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2型糖尿病
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研究疾病代码:
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Target disease:
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Type 2 diabetes
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Target disease code:
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研究类型:
Study type:
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观察性研究
Observational study
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研究设计:
Study design:
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非随机对照试验
Non randomized control
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研究所处阶段:
Study phase:
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探索性研究/预试验
Pilot clinical trial
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研究目的:
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基于临床路径管理,以西医常规治疗作为对照,评价西医常规治疗联合中成药对2型糖尿病患者的糖化血红蛋白、血糖、血脂、体重、BMI、腰围、臀围、腰臀比、抗糖尿病西药减停率、中医症状及延缓糖尿病并发症的疗效,同时评价联合应用的安全性,为糖尿病的中医治疗提供临床证据。
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Objectives of Study:
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Based on clinical pathway management, Western medicine routine treatment as a control, evaluation of Western medicine combined with Chinese patent medicine for type 2 diabetes patients with glycosylated hemoglobin, blood sugar, blood lipids, body weight, BMI, waist circumference, hip circumference, waist-to-hip ratio, anti-diabetes western medicine reduction The rate, the symptoms of TCM and the efficacy of delaying the complications of diabetes, and the safety of combined application, provide clinical evidence for the treatment of Chinese medicine in the diabetes.
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药物成份或治疗方案详述:
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Description for medicine or protocol of treatment in detail:
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纳入标准:
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(1)根据1999年WHO标准,符合2型糖尿病的诊断标准;
(2)年龄18~70岁;
(3)签署患者知情同意书。
(4)患者能提供详细的联络方式,无短期迁移,愿意配合随访。
(5)符合2010年国家中医药管理局医政司《消渴病中医临床路径》、《消渴病中医诊疗方案》、《中药新药临床研究指导原则》规定的肝胃郁热证、阴虚火旺证、气阴两虚证、阴阳两虚证的诊断标准。
(6)经过筛选期(饮食控制+运动疗法控制2周)后,FBG≥7.0mmol/l,但<13.9mmol/l,或餐后2小时血糖≥11.1mmol/l。
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Inclusion criteria
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(1) According to the 1999 WHO standard, meet the diagnostic criteria for type 2 diabetes;
(2) Aged 18 to 70 years;
(3) Sign the patient's informed consent form.
(4) Patients can provide detailed contact information, no short-term migration, and willing to cooperate with follow-up.
(5) Comply with the Drug TCM Clinical Pathway for Diabetes Mellitus, Traditional Chinese Medicine Diagnosis and Treatment Program for Diabetes Mellitus and Guidelines for Clinical Research of New Drugs in Traditional Chinese Medicine in 2010, the liver and stomach stagnation syndrome and yin deficiency fire certificate Diagnostic criteria for qi and yin deficiency syndrome and yin and yang deficiency syndrome.
(6) After screening period (dietary control exercise therapy for 2 weeks), FBG≥7.0mmol/l, but <13.9mmol/l, or 2 hours after meal, blood glucose≥11.1mmol/l.
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排除标准:
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(1)已确诊糖尿病并发症;
(2)有严重的心、肺、肝、肾、脑等并发症者,或合并其他严重原发性疾病者;
(3)血压未经控制或经控制后,收缩压>160 mmHg或舒张压>100 mmHg者;
(4)近1个月内有糖尿病酮症酸中毒或严重感染者;
(5)妊娠期、哺乳期、或准备怀孕的妇女;
(6)肝、肾功能受损者(ALT、AST大于正常值上限2倍;血清肌酐大于正常值上限;
(7)正在参加其他临床试验的患者;
(8)精神病患者,酗酒和/或精神活性物质,药物滥用者和依赖者;
(9)根据研究者的判断,具有降低入组可能性或使入组复杂化的其他病变或情况,如工作环境经常变动、生活环境不稳定等易造成失访的情况;
(10)对本研究了解不充分、不愿参加,或依从性差者;不合作者(不能配合饮食控制,或不按规定用药而影响疗效判定者)。
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Exclusion criteria:
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(1) Diabetes complications have been diagnosed;
(2) Those with serious complications such as heart, lung, liver, kidney and brain, or those with other serious primary diseases;
(3) If the blood pressure is not controlled or controlled, the systolic blood pressure is >160 mmHg or the diastolic blood pressure is >100 mmHg;
(4) Patients with diabetic ketoacidosis or severe infection in the past 1 month;
(5) Women who are pregnant, breastfeeding, or ready to become pregnant;
(6) Those with impaired liver and kidney function (ALT, AST are more than 2 times the upper limit of normal value; serum creatinine is greater than the upper limit of normal value;
(7) Patients who are participating in other clinical trials;
(8) Psychiatric patients, alcohol and/or psychoactive substances, drug abusers and dependents;
(9) According to the judgment of the researcher, other lesions or situations that reduce the possibility of enrollment or complicate the enrollment, such as frequent changes in the working environment and unstable living environment, may cause loss of follow-up;
(10) Those who are not fully aware of this study, are unwilling to participate, or have poor compliance; those who do not cooperate (can not cooperate with diet control, or do not follow the prescribed medication to affect the efficacy judgment).
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研究实施时间:
Study execute time:
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从From
2019-01-01
至To
2021-12-31
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征募观察对象时间:
Recruiting time:
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从From
2019-06-01
至To
2019-12-01
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