IRCT20201230049882N1尚未招募4 期
The assessment of the safety and efficacy of Basalin (Insulin glargine) in patients with type 2 diabetes: a postmarketing survey
Pooyesh darou0 个研究点目标入组 400 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 30 years 至 65 years(—)
- 性别
- All
入选标准
- •Type 2 diabetic patients of both sexes and between 30-65 years of age.
- •Patients who have been treated with oral glucose medications for at least 6 months prior to the start of the study and have not achieved their therapeutic goals (7.5%Patients who have not received Lantus insulin glargine or any long-acting insulin in the last 6 months.
- •Body mass index < 35 kg/m2
- •Glomerular filtration rate more than 30 ml/min.
- •Following a caring diet and exercise regimen recommended by the medical team and tend to maintain them for the entire duration of the study.
排除标准
- •History of diabetic ketoacidosis before the study
- •Hospital admission history more than 2 times due to diabetes in the last 1 year
- •History of brittle diabetes (a condition in which the disease is very difficult to control, as the patient's blood sugar level fluctuates from very low to very high)
- •The presence of any severe complications of diabetes, including end-stage renal disease, advanced coronary artery disease or myocardial infarction during the 6 months prior to the study, or autonomic peristaltic problems, such as gastroparesis.
- •Laboratory disorders at the beginning of the study, such as high levels of liver enzymes more than 3 times above normal limit
- •History of cirrhosis (CHILD C)
- •Uncontrolled thyroid disease
- •History of autoimmune diseases
- •Treatment with glucocorticoids, immunosuppressive or cytotoxic drugs for 60 days prior to enrollment
- •Presence of any active malignancy or history of malignancy
- •History of drug or alcohol abuse (based on patient self-expression)
- •Severe physical and mental disorders
- •Pregnancy, breastfeeding or planning to get pregnant in the next 6 months
- •Simultaneous participation of the patient in another clinical trial or taking any other study drug from 6 months before enrollment
- •History of positive test results for HIV, hepatitis B or hepatitis C, or covid-19
- •History of organ transplantation
研究者
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