跳至主要内容
临床试验/NCT01371045
NCT01371045撤回不适用

Hormonal and Metabolic Responses to Oral Glucose During Somatostatin Analog Use

Cedars-Sinai Medical Center1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2011年6月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
36
试验地点
1
主要终点
Growth hormone response to OGTT

研究概览

简要总结

The purpose of this study is to test the effect of long-acting somatostatin analog medications, taken by patients with acromegaly or carcinoid syndrome, on growth hormone in comparison to healthy controls who are not receiving the medication in order to see whether or not the medication makes the oral glucose test less accurate. The Oral Glucose Tolerance Test (OGTT) is a standard test to measure growth hormone secretion. By comparing GH responses in non-acromegaly subjects taking somatostatin analog treatment, the relative contribution of the medication and the underlying disease state can be analyzed.

详细描述

Subjects will be informed of the study and after providing written informed consent, subjects will be asked to undergo a 2-hour oral glucose tolerance test (ingestion of 75g glucose with subsequent timed assessment of growth hormone, glucose, insulin and related binding proteins.) Baseline assessment of hormones that may contribute to the results will be drawn, prior to performing the test. Patients will be asked to complete one visit total to participate in this trial.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

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

入选标准

  • Diagnosis of acromegaly or carcinoid syndrome
  • Treatment with somatostatin analog therapy (must have established a stable dose of three or more injections on the same dose prior to study enrollment)
  • Healthy control subjects

排除标准

  • Diagnosis of Diabetes Mellitus (Type 1 or Type 2)
  • Use of medication for the treatment of insulin resistance or diabetes

结局指标

主要结局

Growth hormone response to OGTT

时间窗: 2 hours

assessment of the validity of GH suppression during somatostatin analog treatment in acromegaly and non-acromegaly subjects

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

Odelia Cooper

Professor of Medicine

Cedars-Sinai Medical Center

研究点 (1)

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