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临床试验/NCT04240171
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

Damanhour University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年12月1日最近更新:
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:

  1. Approval will be obtained from Research Ethics Committee of Faculty of Pharmacy, Damanhour University.
  2. All participant agreed to take part in this clinical study and provide informed consent.
  3. 60 Patients with type 2 DM will be enrolled Internal Medicine Department, Tanta University Hospital.
  4. Serum samples will be collected for measuring the biomarkers.
  5. 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
  6. All patients will be followed up during 3 months' period.
  7. At the end of 3 months, step 4 will be repeated.
  8. Statistical tests appropriate to the study design will be conducted to evaluate the significance of the results.
  9. 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.
  10. Results, discussion, conclusion, and recommendations will be given.

Methodology:

  1. Fasting blood glucose (FBG) 2 hrs. post prandial blood glucose(2hPPBG) will be measured by glucometer.
  2. 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).
  3. 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

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rehab Werida

Clinical Pharmacy Lecturer

Damanhour University

研究点 (1)

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