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临床试验/NCT05482789
NCT05482789招募中4 期

Pilot Study of Exenatide Pharmacokinetics and Pharmacodynamics in Gestational Diabetes

Maisa N. Feghali, MD1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2023年4月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
13
试验地点
1
主要终点
Area Under the Plasma Concentration Versus Time Curve (AUC) of glucose

研究概览

简要总结

This study is being done to study how exenatide, an FDA-approved drug that lowers blood sugar in non-pregnant patients with type II diabetes, works in pregnant women. To do this, the investigators will study the drug's pharmacokinetics (what the body does to the drug; specifically, how quickly your body breaks down and excretes exenatide) and pharmacodynamics (what the drug does to the body; specifically, how effectively exenatide helps the participants' pancreas secrete insulin and how well it controls blood sugar after a meal). There are only two main drug therapies (insulin injections and glyburide pills) currently used for gestational diabetes and not all women achieve good enough blood sugar control without side effects. Therefore, the investigators hope to find out if exenatide might also be helpful in gestational diabetes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant women (singleton)
  • Gestational diabetes not requiring medical therapy
  • Between 18 and 50 years of age
  • Able to give written informed consent

排除标准

  • Women in the first trimester of pregnancy
  • Hematocrit less than 30%
  • Current or past treatment with any hypoglycemic agent
  • Women with gastrointestinal disease or symptoms consistent with nausea, vomiting, abdominal pain or reflux requiring medical treatment.
  • Women with high triglyceride levels, history of gallbladder or pancreatic disease.
  • Clinical diagnosis or history of any renal insufficiency (or decreased creatinine clearance)

研究组 & 干预措施

Exenatide

Experimental

Participant receives injection of 10 micrograms of Exenatide sub-cutaneously the given mixed meal test and blood samples will be drawn for laboratory testing.

干预措施: Exenatide (Drug)

结局指标

主要结局

Area Under the Plasma Concentration Versus Time Curve (AUC) of glucose

时间窗: Baseline and 1 week later

Glucose concentration over the course of each study visit following mixed tolerance test

次要结局

  • Area Under the Plasma Concentration Versus Time Curve (AUC) of exenatide(1 week after study enrollment)

研究者

发起方
Maisa N. Feghali, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Maisa N. Feghali, MD

Assistant Professor

University of Pittsburgh

研究点 (1)

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