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临床试验/NCT06774807
NCT06774807已完成不适用

Antagonist of the Glucagon-like Peptide 2 (GLP-2) Receptor

University of Copenhagen1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
SMA blood flow

研究概览

简要总结

This project will describe the role of physiological levels of GLP-2 in regulating the blood flow to the intestines and the effect of the antagonist GLP-2(3-33) in blocking these effects of GLP-2.

详细描述

Ten healthy participants will meet fasting and attend four randomized experimental days of MRI-scans of the abdomen. Each day will include subcutaneous injections of GLP-2 or saline and intravenous infusion of either the GLP-2 (3-33) antagonist or saline. The infusion start at timepoint -20, while the subcutaneous injection is given to timepoint 0 and the participant will lay in the scanner in one hour after injection. Eight MR-scans are done repeatedly to measure the blood flow in larger abdominal vessels and four blood samples are taken during the experimental day for analysis of GLP-2(1-33), GLP-2(3-33) and bone markers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age 18-70 years
  • •BMI 19-28 kg/m2

排除标准

  • •Chronic illness that affects the cardiovascular system or gastrointestinal tract
  • •Treatment with medicine or supplements that cannot be paused for 12 hours
  • •Intake of above 14 alcoholic drinks per week or substance abuse
  • •Liver enzymes (ALAT) above 2 times normal values
  • •Decreased kidney function (eGFR below 90 or creatinine levels over reference value)
  • •Low blood percentage (hemoglobin below reference value)
  • •Any condition or disease that the persons responsible for the study find would interfere with the participation of the study.

研究组 & 干预措施

Saline injection + Saline infusion (SAL-SAL)

Placebo Comparator

Saline subcutaneous injection, Intravenous saline infusion (NaCl (9 mg/ml))

干预措施: Saline infusion (Other)

Saline injection + Saline infusion (SAL-SAL)

Placebo Comparator

Saline subcutaneous injection, Intravenous saline infusion (NaCl (9 mg/ml))

干预措施: Saline injection (Other)

GLP-2 agonist injection + Saline infusion (AGO-SAL)

Active Comparator

Subcutaneous injection of GLP-2 (1-33) agonist, Intravenous infusion of saline (NaCl (9 mg/ml))

干预措施: Saline infusion (Other)

GLP-2 agonist injection + Saline infusion (AGO-SAL)

Active Comparator

Subcutaneous injection of GLP-2 (1-33) agonist, Intravenous infusion of saline (NaCl (9 mg/ml))

干预措施: Agonist injection (Other)

GLP-2 agonist injection + GLP-2 1 nmol antagonist infusion (AGO-1ANT)

Experimental

Subcutaneous Injection of GLP-2 (1-33) agonist, Intravenous infusion of 1 nmol/kg/min GLP-2 (3-33) antagonist

干预措施: 1nmol antagonist infusion (Other)

GLP-2 agonist injection + GLP-2 1 nmol antagonist infusion (AGO-1ANT)

Experimental

Subcutaneous Injection of GLP-2 (1-33) agonist, Intravenous infusion of 1 nmol/kg/min GLP-2 (3-33) antagonist

干预措施: Agonist injection (Other)

GLP-2 agonist injection + GLP-2 4 nmol antagonist infusion (AGO-4ANT)

Experimental

Subcutaneous Injection of GLP-2 (1-33) agonist, Intravenous infusion of 4 nmol/kg/min GLP-2 (3-33) antagonist

干预措施: 4 nmol antagonist infusion (Other)

GLP-2 agonist injection + GLP-2 4 nmol antagonist infusion (AGO-4ANT)

Experimental

Subcutaneous Injection of GLP-2 (1-33) agonist, Intravenous infusion of 4 nmol/kg/min GLP-2 (3-33) antagonist

干预措施: Agonist injection (Other)

结局指标

主要结局

SMA blood flow

时间窗: 85 minutes

Blood flow in the superior mesenteric artery

次要结局

  • PVblood flow(85 minutes)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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