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临床试验/NCT07287800
NCT07287800进行中(未招募)1 期

A Prospective Study of Testosterone Supplementation in Hypogonadal Patients Receiving a Renal Transplant

University of California, Los Angeles1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月1日最近更新:
干预措施

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
50
试验地点
1
主要终点
Adverse Events

研究概览

简要总结

This prospective study aims to evaluate the safety and efficacy of testosterone replacement therapy (TRT) as an adjunct to an enhanced recover after surgery (ERAS) protocol in men with end-stage renal disease (ESRD) undergoing kidney transplantation.

Participants will be highly-listed hypogonadal men, defined as total testosterone level <300 on two occasions with clinical symptoms of hypogonadism, with ESRD who are expected to receive a kidney transplant within 6 months. Participants will be started on TRT, ideally for at least 3 months prior transplantation. The investigators will perform a subset analysis to evaluate if there is a significant difference in our endpoints by comparing these two subgroups (Three months or more receiving TRT vs. Less than three months receiving TRT). There will be no cut-off time for pre-transplant TRT. Following the intervention period, a historical control cohort of age-matched and health-matched patients will be identified, who have followed a standard transplant protocol that does not incorporate TRT. The primary outcome will evaluate safety, including 30- and 90-day adverse events, 3, 6, and 12-month allograft survival, and overall patient survival. Secondary outcomes will focus on (1) qualitative assessments of symptoms using validated questionnaires, (2) quantitative improvements in the hormonal profile before and after initiation of TRT and surgery, and (3) allograft function and incidence of delayed graft function. The results of this study could provide novel insights into the benefits of TRT in improving surgical outcomes in men with ESRD undergoing kidney transplantation.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Male patients older than 18 years old with confirmed end-stage renal disease (ESRD).
  • Hypogonadal (testosterone level <300 ng/dL) with clinical symptoms of hypogonadism.
  • Expected to undergo kidney transplantation within a 6-month period.
  • Able and willing to comply with study procedures and follow-up visits.

排除标准

  • Women or non-hypogonadal men.
  • Any contraindications to testosterone therapy, including:
  • History of Breast Cancer
  • Severe untreated OSA
  • Polycythemia (Hct >54%)
  • Uncontrolled chronic heart failure (CHF)
  • A history of a Major Adverse Cardiac Event (MACE) within the past 6 months
  • Interest in fertility within 1 year
  • An unevaluated PSA >4.0 ng/mL or a PSA >3.0 ng/mL in individuals with risk factors for prostate cancer defined as:
  • Men with African ancestry
  • Men with first-degree relative with prostate cancer
  • Known genetic mutations including BRCA1/2
  • A history of Lynch Syndrome
  • Abnormal DRE
  • Participants already receiving testosterone or other androgen therapies.
  • Severe cardiovascular or pulmonary conditions that pose a high surgical risk.
  • Any condition that, in the opinion of the investigator, would make the subject ineligible for the study.

研究组 & 干预措施

Testosterone Replacement Therapy

Experimental

干预措施: Testosterone Replacement Therapy (Drug)

结局指标

主要结局

Adverse Events

时间窗: 18 months

Complications categorized by the CTCAE classification (grades 1-5)

Overall Survival

时间窗: 18 months

measured as a rate

Death-Censored- Graft Survival

时间窗: 18 months

Graft Survival will be the duration from transplantation until graft failure. Graft failure defined as (1) resumption of dialysis (2) allograft removal or (3) need for retransplantation/relisted on the transplant list

Healthcare Utilization Metrics

时间窗: 18 months

Hospital readmission rates

Length of hospitalization

时间窗: 18 months

days

次要结局

  • Serum Creatinine Levels(At 3-, 6-, and 12-months post-transplantation)
  • estimated glomerular filtration rate (eGFR)(At 3-, 6-, and 12-months post-transplantation)
  • Rate of delayed graft function(1 week following transplant)
  • Tacrolimus trough level(1 month after TRT initiation, and at 3-, 6-, and 12-months post-transplant)
  • Follicle-Stimulating Hormone (FSH)(Once prior to initiation of TRT surgery)
  • Serum Testosterone Panel(Every 3 months after starting TRT; at the time of transplantation; 30-, 90-, 180-, 270-, and 360-days post transplantation)
  • Prostate Specific Antigen (PSA)(at baseline prior to TRT therapy, and every 3-6 months during active hormone therapy.)
  • Luteinizing Hormone (LH)(Once prior to initiation of TRT surgery)
  • Prolactin(Once prior to initiation of TRT surgery)
  • Hemoglobin(1 month after TRT initiation, and at 3-, 6-, and 12-month intervals)
  • Hematocrit(1 month after TRT initiation, and at 3-, 6-, and 12-month intervals)
  • Muscle Body Composition Analysis(at time of consent, 30 days, 180-days, and 360 days after transplantation)
  • Qualitative Assessment of Hypogonadal Symptoms(at time of consent; every 3-6 months starting TRT; 30- and 90-days following transplantation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nima Nassiri

Assistant Clinical Professor of Urology

University of California, Los Angeles

研究点 (1)

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