跳至主要内容
临床试验/NL-OMON31110
NL-OMON31110已完成不适用

A glucagon challenge in healthy volunteers - A glucagon challenge in healthy volunteers

Centre for Human Drug Research0 个研究点目标入组 8 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
8

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Able and willing to provide written informed consent
  • - Age 18 to 65 years
  • - Males or females

排除标准

  • - Clinically significant abnormalities in medical history, physical examination or
  • laboratory examination
  • - Pregnanant or breast feeding females
  • - Not able or willing to use an acceptable contraceptive method for study duration
  • for females (hormonal contraceptives, intra-uterine device or condom/pessary)
  • - Not able and willing to refrain from smoking and/or xanthine use on study day
  • - Fasting plasma glucose at screening >= 6.4
  • - HbA1C >= 7%
  • - BMI >= 30 kg/m2
  • - Hypertension (systolic blood pressure >= 140 mm Hg or a diastolic blood pressure >=
  • - Suspicion of a pheochromocytoma (i.e. Rapid heart rate, palpitations, excessive
  • sweating, chest pain, upper abdominal pain, severe headaches, tremors, feeling
  • of anxiety or extreme fright, pale skin)
  • - Positive urine testing for cocaine, opiates (morphine) and/or THC at screening
  • - Use of concomitant medication (except hormonal contraceptives)
  • - Positive test result for HIV, hepatitis B virus, and/or hepatitis C virus
  • - History of alcohol or drug abuse
  • - Undergoing or have undergone treatment with another investigational drug,
  • biologic agent or device within 90 days prior to Screening.
  • - Blood donation within three months of screening

研究者

相似试验