跳至主要内容
临床试验/EUCTR2006-003101-53-DE
EUCTR2006-003101-53-DE进行中(未招募)不适用

A randomised placebo controlled study of transdermal testosterone therapy (testosterone 1% hydroalcohol gel) to investigate the efficacy and safety in men with abdominal obesity, low testosterone levels and early stages of the metabolic cluster syndrome. - ARTinMMS

Karolinska Institutet0 个研究点目标入组 176 人开始时间: 2007年1月30日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
176

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • 1. Male 30 to 70 years (inclusive)
  • 2. Metabolic syndrome defined according to the International Diabetes Foundation
  • a) Abdominal obesity (waist circumference > 94 cm for European men) and any two of the following criteria
  • b) Triglycerides > 1.7 mmol/L or specific treatment for this
  • c) HDL < 1.03 nmol/L or specific therapy for this
  • d) Systolic blood pressure = 130 mmHg or diastolic BP = 85 mmHg or treatment for this.
  • e) Fasting plasma glucose = 5.6 mmol/L
  • or previously diagnosed type 2 diabetes mellitus defined by:
  • Fasting plasma glucose = 7.8 mmol/L on two occasions, or random glucose = 11.1 mmol/L and classic symptoms of type 2 diabetes
  • 3.Impaired glucose tolerance
  • If the definition of the metabolic syndrome, as described above, is fulfilled but fasting plasma glucose < 5.6 mmol/L the result of an oral glucose tolerance test must be classified as reduced glucose tolerance with a venous blood glucose 7.8 - 11.1 mmol/L or higher 120 min after intake of 75 g of glucose in a water solution (2h OGTT) (www.diabetes.org/main/info/pre-diabetes.jsp)
  • 4.Hypogonadism defined as a S-Testosterone <= 12 nmol/L taken at 8:00-10:00 a.m. and less than 2 months before inclusion in the study.
  • 5.Screening value of HbA1c < 8.0 %
  • 6.Weight below and inclusive 120 kg
  • 7.Body Mass Index (BMI) below and inclusive 40
  • 8.Hematocrit below and inclusive 50%
  • 9.Signed Written informed consent obtained
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.Insulin therapy and treatment with glitazones.
  • 2.Use of androgen therapy or anabolic steroids within 6 months of entry into the study.
  • 3.Known congestive heart failure, progressing angina pectoris or a history of myocardial infarction within the last 12 months.
  • 4.Known untreated pituitary disease.
  • 5.A history of significant renal or liver disease or any malignancy.
  • 6.Any disease requiring long-term use of drugs interfering with androgens; spironolactone, Ketoconazol, corticosteroids, cimetidin, fentiazines, tricyclic antidepressives, anabolic steroids, 5-alfa reductase inhibitors, antiestrogens.
  • 7.Prostate Specific Antigen (PSA) >= 4 ng/ml.
  • 8.Suspected malignancy after prostata palpation, unless biopsy shows the opposite.
  • 9.Malignant tumour of the mammary gland
  • 10.Ongoing micturition problem severely affecting patient’s daily living at the discretion of the investigators judged by the investigator.
  • 11.Any contraindication for treatment with testosterone 1% hydroalchol gel according to the labelling as well as known or suspected allergy to the specific product used in the study.
  • 12.Contagious blood disease.
  • 13.Known alcohol or drug abuse, or any condition associated with poor compliance.
  • 14.Participation in a clinical study during the last 90 days before start of treatment.
  • 15.Previous enrolment or randomisation in the present study.

研究者

相似试验