跳至主要内容
临床试验/KCT0001608
KCT0001608招募中未知

Effect of administration of androgen in cardiovascular system in male hypogonadism

Chonbuk National University Hospital0 个研究点目标入组 89 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
89

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
18(Year) 至 80(Year)(—)
性别
Male

入选标准

  • 1). The study population is comprised of hypogonadal patients who visit to the Chonbuk National University Hospital and has testosterone deficiency syndrome and has 18 to 80 years old of age.
  • 2). On screening, the patient who has lower total testosterone level less than 2.5 ng/ml.
  • 3). On screening, the patient who has lower level less than 18 g/dl of hemoglobin.
  • 4). On screening, the patient who has lower level less than 52% of hematocrit.
  • 5). The patient agree to the study after the patient listen the explanation about the study.
  • 6). In androgen deficiency in the aging male (ADAM) questionnaire, the patient who has positive answer to the question about sexual dysfunction, or has positive answer to other 2 questionnaires.

排除标准

  • 1). The patient who has not treated for specific disease for 5 years.
  • 2). The patient who has been administered androgen for recent 3 months.
  • 3). The patient who has treated with antiandrogen in recent 3 months.
  • 4). The patient who has the abnormal laboratory data;
  • AST and ALT are over 2 times more than upper limit of normal range
  • Serum creatinine is over more than 2.0 mg/dl
  • Creatine Kinase is over 2 times more than upper limit of normal range.
  • 5). The patient who was administered corticosteroid in recent 3 months.
  • 6). The patient who was transfused whole blood or constituent donation in recent 3 months.
  • 7). The patient who drink severe amount of alcohol over 21 units/week
  • 8). The patient who was join the other clinical trial 1 month before this clinical trial.
  • 9). The patient who has prostate specific antigen (PSA) level more than 4 ng/ml (However, the patient who has not been identified to prostate cancer by the biopsy can be enrolled the study).
  • 10). The patient who has prostate cancer
  • 11). The patient who has severe benign prostate hyperplasia (BPH) (the volume is more than 60 ml and maximal uroflow rate is less than 5 ml/ sec.)
  • 12). The patient who has abnormal laboratory data and is not good for the clinical trial.

研究者

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