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临床试验/NCT04729582
NCT04729582尚未招募1 期

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

Simone Spuler, MD4 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2024年6月最近更新:
适应症

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

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

发起方
Simone Spuler, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Simone Spuler, MD

Principal investigator

Charite University, Berlin, Germany

研究点 (4)

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