ACTRN12624000345583招募中2 期
Testosterone treatment for the management of fatigue in ambulatory patients with advanced cancer: A pilot feasibility double-blind placebo-controlled study
niversity of Technology Sydney0 个研究点目标入组 26 人开始时间: 2024年3月26日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 26
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Adult men and women with advanced cancer, solid organ or haematopoietic malignancy
- •18 years or older
- •The Palliative Care Outcome Collaboration (PCOC) Symptom Assessment Score (SAS) of 3 or greater for fatigue
- •Australia - modified Karnofsky Performance Status Palliative Score of 40 or above
- •Able to give informed consent as determined by the treating clinician
- •Able to complete study procedures and comply with study procedures
- •No indication of primary hypogonadism on the completion of the screening reproductive function questionnaire
排除标准
- •Advanced prostate carcinoma, or current diagnosis of prostate carcinoma receiving active hormonal therapy.
- •Baseline erythrocytosis (haematocrit >50%)
- •Primary male hypogonadism
- •Previous adverse reaction to Testosterone Treatment
- •Pregnant or breastfeeding
- •AKPS of 30 or below.
- •Patients with advanced breast carcinoma if the treating Oncologist objects
- •Allergy or hypersensitivity to Almond oil or tree nuts.
- •Unable to give informed consent.
研究者
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