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临床试验/NCT00917449
NCT00917449已完成3 期

Interventional Pharmacological Study With L-Arginine in the Prevention of Type 2 Diabetes Mellitus in Patients With Metabolic Syndrome

IRCCS San Raffaele1 个研究点 分布在 1 个国家目标入组 142 人开始时间: 2005年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
142
试验地点
1
主要终点
To evaluate the efficacy of long term (18 months) L-Arginine therapy in preventing or delaying clinical onset of type 2 diabetes mellitus in subjects with impaired glucose tolerance (IGT) and Metabolic Syndrome.

研究概览

简要总结

Aim

The principal objective of this project is:

• To evaluate the efficacy of long term (18 months) L-Arginine therapy in preventing or delaying clinical onset of type 2 diabetes mellitus in subjects with impaired glucose tolerance (IGT) and Metabolic Syndrome.

Secondary end points are:

  1. To define if a long term treatment with L-arginine is able to ameliorate insulin sensitivity and endothelial dysfunction in this population.
  2. To find new risk profiles and candidate genes able to define the sub-group of patients at higher risk to develop type 2 diabetes mellitus.

Methodology This is a double blind, parallel, one centre study to determine if long term oral L-arginine administration is able to delay or prevent type 2 diabetes mellitus in patients with Metabolic Syndrome. Two hundred and ninety four subjects were recruited at the Cardio-Metabolic and Clinical Trials Unit of the San Raffaele Scientific Institute. One hundred and forty two patients were randomized to enter the study and assigned to two arms: oral L-arginine (6.4 g/die) or placebo, in addition to diet and physical exercise. The treatment were maintained for 18 months. Visits were performed every 3 months for clinical evaluation, blood samples, treatment supply and collection of data on adverse events. Furthermore, patients were contacted every month by telephone to evaluate the accurate continuation of the study and they were instructed to phone to the centre in case of possible adverse events.

An OGTT were performed before the enter into the study and at the end of the study period. An additional OGTT were performed at an intermediate visit if fasting glucose levels were more than 126 mg/dl. A diabetic response caused the end-point of the patient. Metabolic, hormonal and endothelial activation and inflammation parameters were measured. Evaluation of endothelium-mediated and non-endothelium-mediated vasodilatation were performed by strain gauche plethysmography evaluating forearm blood at the basal state. in post-ischemic conditions and after nitroglycerine administration.

Before the enter into the study, an additional blood sample were drawn for DNA extraction and candidate genes variants evaluation. Before the enter into the study and at the end of the study period, gene expression for inflammation were measured on mRNA extraction on endothelial progenitor cells.

详细描述

This is a double blind, parallel, one centre study to determine if long term oral L-arginine administration is able to delay or prevent type 2 diabetes mellitus in patients with IGT and Metabolic Syndrome. Two hundred and ninety four subjects were recruited at the CardioMetabolic and Clinical Trials Unit of the San Raffaele Scientific Institute. One hundred and fourty two patients were randomized to enter the study. Patients were randomly assigned to two arms: oral L-arginine (6.4 g/die) or placebo in blind scheme. The treatment were maintained for 18 months. Visits will be performed every 3 months for clinical evaluation, blood samples, treatment supply and collect data on adverse events, if any. Furthermore, patients were contacted every month by telephone to evaluate the accurate continuation of the study and they were instructed to phone to the centre in case of possible adverse events.

Inclusion criteria

  • Written informed consent must be obtained before any procedure of the study is done.
  • Male or Female aged more than 35 years.
  • Diagnosis of IGT after a standard Glucose Tolerance Test (OGTT, 75 g)
  • Moreover, in order to be considered affected by Metabolic Syndrome, they must have two or more of the following criteria:
  • Abdominal obesity (waist>120 cm for man, >88 cm for women)
  • Hypertriglyceridemia (>150 mg/dl)
  • Low HDL cholesterol (<40mg/dl in man, <50 mg/dl in woman)
  • Hypertension (>130 / >85 mmHg) Exclusion criteria
  • Presence of type 1 or type 2 diabetes mellitus
  • Fasting glucose levels >126 mg/dl
  • Sitting Systolic Arterial Pressure >140mmHg, and Sitting Diastolic Arterial Pressure >90mmHg
  • Pregnancy
  • Known renal insufficiency or creatinine levels more than 1.8 mg/dl,
  • Presence of chronic hepatopathy or levels of ALT and AST more than two standard deviations from normality levels
  • Presence of malignancy
  • Abuse of alcohol or abuse substances
  • Psychiatric disorders

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • Written informed consent must be obtained before any procedure of the study is done.
  • Male or Female aged more than 35 years.
  • Diagnosis of IGT after a standard Glucose Tolerance Test (OGTT, 75 g)
  • Moreover, in order to be considered affected by Metabolic Syndrome, they must have two or more of the following criteria:
  • Abdominal obesity (waist>120 cm for man, >88 cm for women)
  • Hypertriglyceridemia (>150 mg/dl)
  • Low HDL cholesterol (<40mg/dl in man, <50 mg/dl in woman)
  • Hypertension (>130 / >85 mmHg)

排除标准

  • Presence of type 1 or type 2 diabetes mellitus
  • Fasting glucose levels >126 mg/dl
  • Sitting Systolic Arterial Pressure >140mmHg, and Sitting Diastolic Arterial Pressure >90mmHg
  • Pregnancy
  • Known renal insufficiency or creatinine levels more than 1.8 mg/dl,
  • Presence of chronic hepatopathy or levels of ALT and AST more than two standard deviations from normality levels
  • Presence of malignancy
  • Abuse of alcohol or abuse substances
  • Psychiatric disorders

研究组 & 干预措施

L-arginine

Active Comparator

L-arginine (3.2 gr bid) plus lifestyle counselling vs placebo plus lifestyle counselling

干预措施: L-arginine (Drug)

placebo

Placebo Comparator

placebo plus lifestyle counselling for 18 months

干预措施: Placebo (Drug)

结局指标

主要结局

To evaluate the efficacy of long term (18 months) L-Arginine therapy in preventing or delaying clinical onset of type 2 diabetes mellitus in subjects with impaired glucose tolerance (IGT) and Metabolic Syndrome.

时间窗: 18 months

次要结局

  • Define if the treatment with L-arginine can ameliorate insulin sensitivity and endothelial dysfunction and find new risk profiles and candidate genes able to characterize the sub-group of patients at higher risk to develop type 2 diabetes mellitus.(18 months)

研究者

申办方类型
Other

研究点 (1)

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