Combined Phase 1 and 1/2a Clinical Trial Evaluating the Safety and Efficacy of an Autologous Muscle Stem Cell Therapy in the Treatment of Urinary Incontinence in Isolated Epispadias
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 21
- 试验地点
- 4
- 主要终点
- Prevalence of Intervention-related Adverse Events
研究概览
简要总结
The aim of this trial is to evaluate the safety and efficacy of an autologous muscle stem cell therapy in the treatment of congenital urinary incontinence in isolated epispadias.
详细描述
Epispadias is the mildest form of exstrophy-epispadias complex (EEC); a congenital malformation disorder involving the midline abdominal and genitourinary structures. Patients with epispadias have a defect in the urethral sphincter resulting in urinary incontinence. This trial investigates the injection of autologous primary human muscle stem cells into the urethral sphincter with the aim of repairing the defect and restore the anatomic ability for continence.
Eligible participants will undergo muscle biopsy during a routine cystoscopy. Acquired muscle tissue is used for the isolation and expansion of muscle stem cells ex-vivo. Muscle stem cells are injected into the urethral sphincter under visual control using cystoscopy. Participants are assessed for safety and efficacy for a minimum of 12 months post-intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 3 Years 至 17 Years(Child)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Isolated epispadias
- •Aged ≥ 3 years
- •Urinary incontinence as defined according to the International Children´s Continence Society
- •Informed consent
排除标准
- •Acute or chronic inflammatory local or systemic disease
- •Coagulation Disorder
- •Previous adverse reaction to anesthesia
- •Congenital heart defect, cardiac arrhythmia
结局指标
主要结局
Prevalence of Intervention-related Adverse Events
时间窗: Upto 12 months post-intervention
Characterization of type, incidence, severity, and duration of adverse events
Change in Leak Point Pressure (LPP)
时间窗: Six months post-intervention
Change in LPP is calculated from baseline measurement
次要结局
未报告次要终点
研究者
Simone Spuler, MD
Principal investigator
Charite University, Berlin, Germany
