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临床试验/NCT03351634
NCT03351634尚未招募不适用

EVALUATION OF THE SAFETY AND EFFICACY OF ADJUSTABLE CONTINENT THERAPY FOR THE MANAGEMENT OF NEUROGENIC INCONTINENCE IN CHILDREN WITH SPINAL DYSRAPHISM.

Assistance Publique Hopitaux De Marseille2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2017年12月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
10
试验地点
2
主要终点
Measurement of urinary continence with the Schulte-Baukloh score and 24hours pad-test

研究概览

简要总结

Urinary continence is still a difficult goal to achieve in neurogenic bladder patients. Conservative treatment of neurogenic urinary incontinence using clean intermittent catheterization in conjunction with pharmacological therapy, notably anticholinergic medication +/- adrenergic agents, may produce continence in a variable number of patients. In other patients, reconstructive surgery of the bladder and/or bladder neck is necessary to achieve urinary continence. Surgical treatment options to increase bladder outlet resistance in patients with neurogenic bladder include injection of bulking agents around the bladder neck, bladder neck reconstruction, fascial sling procedures and Artificial Urinary Sphincter.

The Adjustable Continence Therapy system (ACT) or periurethral adjustable balloons are a minimally invasive device consisting of two volume-adjustable balloons implanted periurethrally at the bladder neck as a method of augmenting titration for urethral coaptation. Adjustable means that such system would be adaptable to the individual clinical condition.

Originally conceived and developed as a treatment for female stress urinary incontinence, the technique has been then adapted and balloons were globally developed for the use in postprostatectomy incontinence. The published success rate in male after prostatectomy and in women was respectively 56 to 92% and 60 to 83%.

The investigators hypothesize that the use of ACT for treating incontinence in children secondary to neurogenic sphincter incontinence could compress the urethra or the bladder neck, acting as an extrinsic occlusive system increasing passive and dynamic urethral and bladder resistance.

Goal of the study:

To prospectively assess the efficacy and safety of periurethral adjustable balloons in the treatment of neurogenic incontinence in children with spinal dysraphism.

Material and methods :

A prospective study will be performed at La Timone Enfants hospital and La Nord hospital in Marseille, France. Boys and girls at least at school age (5 or 6 years) with neurogenic incontinence due to outlet issues (low detrusor leak point pressure and low stress leak point pressure) with spinal dysraphism will be recruited.

The ACT balloon is an implantable medical device developed and furnished for free by Uromedica (Irvine, CA, USA). The procedure is performed under general anaesthesia using the same implantation technique as published in adult population.

研究设计

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

入排标准

年龄范围
5 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Boys and girls > 5 years with spinal dysraphism (occult or open)
  • Neurogenic sphincteric incontinence (leak point pressure < 45 cm d'H20, open bladder neck during filling, urinary incontinence)
  • Normal renal function (eGFR > 90ml/min)
  • No (or stable) upper urinary tract dilatation in ultrasound
  • In case no compliante bladder ( bladder capacity < 50% for the age) a concomitant injection of botox endoscopically will be performed

排除标准

  • under 5 years with an acquired neurogenic bladder
  • renal insufficiency (acute or chronic)
  • evolutive deterioration of the upper urinary tract (hydronephrosis)
  • active systemic or urinary tract infections
  • unmanageable detrusor instability
  • reduced bladder compliance
  • residual volume greater than 100 ml after voiding
  • bleeding disorders
  • urethral stenosis
  • who refused CIC
  • patent sacral bedsore

研究组 & 干预措施

Children with neurogenic incontinence with spinal dysraphism

Experimental

干预措施: Implantation of ACT balloon, Uromedica (Irvine, CA, USA) periurethrally at the bladder neck (Device)

结局指标

主要结局

Measurement of urinary continence with the Schulte-Baukloh score and 24hours pad-test

时间窗: 5 YEARS

Evaluation of urinary continence with mictional schedule and 24hours pad-test (Patients will be classified as "dry" if they will be using no pads or a single ''security pad'' per day; "significantly improved" if a reduction \>50% in pad usage (usually representing 2- 5 pads/day, depending on preoperative pad use); and little/no improvement (\>5 pads/day and \<50% improvement against baseline) and the Schulte-Baukloh score

次要结局

  • Evaluation of the quality of life with the PIN-Q score(5 YEARS)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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