KCT0001608招募中未知
Effect of administration of androgen in cardiovascular system in male hypogonadism
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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