NCT04240171已完成不适用
Comparative Study of Dapagliflozin Versus Glimepiride Effect on Insulin Regulated Aminopeptidase (IRAP) and Interleukin-34 (IL-34) in Patient With Type 2 Diabetes Mellitus
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Blood Sugar (mg/dl)
研究概览
简要总结
Research objectives:
The aim of the study to check the effect of Dapagliflozin versus Glimepiride on insulin regulated aminopeptidase (IRAPe), NT-Pro BNP and interleukin-34 (IL-34) in patients with type 2 diabetes mellitus, and associated it with insulin resistance.
详细描述
Method and proposal steps:
- Approval will be obtained from Research Ethics Committee of Faculty of Pharmacy, Damanhour University.
- All participant agreed to take part in this clinical study and provide informed consent.
- 60 Patients with type 2 DM will be enrolled Internal Medicine Department, Tanta University Hospital.
- Serum samples will be collected for measuring the biomarkers.
- All enrolled 60 patients will be mentioned as two groups; Group 1(n=30): are the patients who are prescribed dapagliflozin to control their blood sugar level. Group 2 (n=30): are the patients who are prescribed glimepiride
- All patients will be followed up during 3 months' period.
- At the end of 3 months, step 4 will be repeated.
- Statistical tests appropriate to the study design will be conducted to evaluate the significance of the results.
- Measuring outcomes: the primary outcome is the change from baseline to post-treatment insulin sensitivity reflected by change of serum level of measured marker after 3 months.
- Results, discussion, conclusion, and recommendations will be given.
Methodology:
- Fasting blood glucose (FBG) 2 hrs. post prandial blood glucose(2hPPBG) will be measured by glucometer.
- HbA1c %, Fasting plasma insulin (FPI), Interleukin-34 (IL-34), NT-Pro BNP and extracellular domain of insulin regulated aminopeptidase (IRAPe) will be assayed by Enzyme-Linked Immunosorbent Assay (ELISA).
- Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) will be calculated.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 35 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •60 Patients with type 2 DM diagnosed clinically. The age ranged from 18 to 70 years. There are no limits to the duration of DM and gender.
排除标准
- •Other types of DM
- •Hypersensitivity to the drug
- •Abnormal liver function
- •Patients with renal impairment (eGFR ≤ 60 ml/min)
- •Previous history of bladder cancer
研究组 & 干预措施
dapagliflozin
Group 1(n=30): are the patients who are prescribed dapagliflozin to control their blood sugar level.
干预措施: Dapagliflozin 5Mg Tab (Drug)
glimepiride
Group 2 (n=30): are the patients who are prescribed glimepiride
干预措施: Glimepiride 4Mg Tab (Drug)
结局指标
主要结局
Blood Sugar (mg/dl)
时间窗: three months
serum blood glucose
HbA1c %
时间窗: three months
Glycated Hemoglobin
次要结局
- IRAPe (ng/ml)(Three Months)
- NT-Pro BNP (ng/ml)(Three Months)
- IL-34 (pg./ml)(Three Months)
研究者
Rehab Werida
Clinical Pharmacy Lecturer
Damanhour University
研究点 (1)
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