jRCTs052230106招募中不适用
The utility of penile rehabilitation with vacuum constriction device after performing brachytherapy for prostate cancer. (VIGOR Study)
未提供0 个研究点目标入组 30 人开始时间: 2024年6月5日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 主要终点
- -
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
- Single Arm Study
- 干预模型
- Single Assignment
- 主要目的
- Prevention Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 20age old over 至 75age old under(—)
- 性别
- Male
入选标准
- •Disease: Prostate cancer
- •Stage: Stage 1-2
- •Age: 20-75 years old
- •Gender: Male
- •ECOG PS (Performance Status) 0-1
- •Mild to moderately preserved sexual function before brachytherapy (SHIM more than 12 points)
- •Patients treated with brachytherapy alone
- •Patients planning to have sexual intercourse before or after surgery
- •Patients who have given written consent to participate in this clinical study
排除标准
- •Patients with cognitive impairment
- •Patients with poorly controlled diabetes mellitus (HbA1c of 10% or higher)
- •Patients with neurological disease
- •Patients undergoing adjuvant hormonal therapy (surgical castration or medical castration) for brachytherapy
- •Patients receiving external radiation therapy as adjuvant therapy to brachytherapy
- •Patients taking PDE5 inhibitors
- •Patients using vacuum constriction device
- •Patients on antithrombotic therapy or predisposed to bleeding
- •Patients who have difficulty operating vacuum constriction device
- •Patients who are deemed inappropriate as research subjects by the principal investigator or subinvestigator
结局指标
主要结局
-
SHIM score at 6 months after brachytherapy
次要结局
未报告次要终点
研究者
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