New England Research Institutes, Inc., Watertown, MA 02471, USA.
Aging Male. 2013 Mar;16(1):1-7. doi: 10.3109/13685538.2013.765403. Epub 2013 Feb 4.
Despite the prevalence of hypogonadism (HG) and widespread use of testosterone therapy, little is known about the safety/effectiveness of long-term testosterone use. The Registry of Hypogonadism in Men (RHYME) is a multi-national patient registry assessing prostate health and other outcomes associated with testosterone treatment in men.
Observational patient disease registry.
RHYME is a non-interventional disease registry with longitudinal data collection on a large sample (N = 999) of well-characterized, hypogonadal men aged 18 years or older. The Registry will prospectively evaluate male patients diagnosed with HG, who have not previously been treated with testosterone therapy. Key design features include: (1) broad inclusion/exclusion criteria, (2) standardized central laboratory hormone assays, (3) independent adjudication of prostate biopsies and mortalities, (4) standard of care treatment, (5) comprehensive medical record and questionnaire data at six months and annually post-enrollment and (6) adequate statistical power for assessing prostate endpoints at 36 months.
A total of 25 clinical sites in six European countries (Germany, Italy, the Netherlands, Spain, Sweden and the United Kingdom) have completed recruitment for the study. Recruitment was initiated in May 2009, and completed in December 2011. Data collection is ongoing with a minimum of two years of follow-up on all patients.
尽管低促性腺激素性性腺功能减退症(HG)较为普遍,且睾酮治疗广泛应用,但对于长期使用睾酮的安全性/有效性却知之甚少。男性性腺功能减退症注册研究(RHYME)是一个多国家患者注册研究,评估了前列腺健康和其他与男性睾酮治疗相关的结局。
观察性患者疾病注册研究。
RHYME 是一个非干预性疾病注册研究,对大量特征明确的、年龄在 18 岁或以上的低促性腺激素性男性患者(N=999)进行了长期纵向数据收集。该注册研究将前瞻性评估此前未接受过睾酮治疗的 HG 男性患者。主要设计特点包括:(1)广泛的纳入/排除标准;(2)标准化的中心实验室激素检测;(3)对前列腺活检和死亡率进行独立裁决;(4)标准治疗;(5)在入组后 6 个月和每年进行全面的病历和问卷数据收集;(6)有足够的统计效能在 36 个月时评估前列腺终点。
该研究在六个欧洲国家(德国、意大利、荷兰、西班牙、瑞典和英国)的 25 个临床中心完成了招募。研究于 2009 年 5 月启动,2011 年 12 月完成招募。所有患者的随访时间至少为 2 年,数据收集正在进行中。