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临床试验/NCT04958109
NCT04958109已完成1 期

Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Oral Glucose Tolerance Test

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2021年10月28日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
16
试验地点
1
主要终点
Oral Glucose Sensitivity Index (Kisspeptin-Placebo)

研究概览

简要总结

The goal of this study is to understand how exogenous kisspeptin affects metabolism by evaluating responses to an oral glucose tolerance test

详细描述

Assignment: Each study subject will serve as their own control. The order of the visits will be randomized.

Delivery of Interventions:

  • Prior to the study visit, subjects will undergo a review of their medical history and screening laboratories.

  • During the inpatient study, the subjects will

  • Undergo a 16-hour kisspeptin infusion

  • Undergo an oral glucose tolerance test

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • over the age of 18,
  • normal pubertal development
  • stable weight for previous three months,
  • normal body mass index (BMI between 18.5-25)
  • regular menstrual cycles
  • Physical examination:
  • systolic BP < 140 mm Hg, diastolic < 90 mm Hg
  • Laboratory studies: (per Massachusetts General Hospital reference ranges)
  • normal hemoglobin
  • hemoglobin A1C < 6.5%
  • blood urea nitrogen, creatinine not elevated
  • aspartate aminotransferase, alanine aminotransferase < 3x upper limit of normal

排除标准

  • active illicit drug use,
  • history of a medication reaction requiring emergency medical care,
  • difficulty with blood draws.
  • history of chronic disease, except well controlled thyroid disease,
  • recent use of prescription medications which interfere with metabolism or reproduction (recent = within 5 half-lives of the drug). Use of levothyroxine or seasonal allergy medications is acceptable,
  • history of diabetes in a first degree relative,
  • use of contraceptive pills, patches or vaginal rings within last 4 weeks.
  • hyperlipidemia by fasting lipid panel
  • positive serum pregnancy test (for all women)

研究组 & 干预措施

Kisspeptin

Experimental

• Intravenous administration of kisspeptin 112-121 x 16 hours

干预措施: Oral Glucose Tolerance Test (Diagnostic Test)

Kisspeptin

Experimental

• Intravenous administration of kisspeptin 112-121 x 16 hours

干预措施: Kisspeptin (Drug)

Placebo

Placebo Comparator

• Intravenous administration of placebo x 16 hours

干预措施: Oral Glucose Tolerance Test (Diagnostic Test)

Placebo

Placebo Comparator

• Intravenous administration of placebo x 16 hours

干预措施: Placebo (Drug)

结局指标

主要结局

Oral Glucose Sensitivity Index (Kisspeptin-Placebo)

时间窗: 3 hours

Change in Oral glucose Sensitivity Index between kisspeptin and placebo arms in oral glucose tolerance test

次要结局

未报告次要终点

研究者

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

Stephanie B. Seminara, MD

Chief, Reproductive Endocrine Unit; Professor of Medicine, Harvard Medical School; Director, Harvard Reproductive Endocrine Sciences Center

Massachusetts General Hospital

研究点 (1)

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