Efficacy of Intravesical Oxybutynin in Children With Neurogenic Bladder Dysfunction

ConditionSpina Bifida
Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age6-17
SponsorCentral Hospital, Nancy, France

About this trial

Malformation of the lumbosacral region (spina bifida) affects the innervation of the bladder in children. The usual evolution leads to a neurological bladder with small capacity, poor compliancy and overactivity, exposing to incontinence and obstruction to the evacuation of urine. It is responsible for renal failure requiring dialysis and transplantation. Current therapeutics aim to evacuate urine and reduce intravesical pressure. It gradually combines 1) intermittent catheterization, 2) anticholinergics, 3) botulinum toxin (Botox®) injection into the detrusor (bladder muscle) by cystoscopy and 4) surgery (vesicostomy, Bricker, enterocystoplasty). Oxybutynin relaxes the detrusor, improves continence and reduces intravesical pressure. It is usually administered per os, but there are contraindications (glaucoma, myasthenia), side effects (constipation, dry mouth). It can be difficult to swallow for children, and drug resistance may develop. It can lead to ineffective treatment requiring therapeutic escalation. The next step, intradetrusor Botox® injection, is invasive (cystoscopy), has a limited duration of action (6 months) and must be performed under general anesthesia in children.

Surgical treatments are effective but irreversible and responsible for morbidity and mortality. A randomized study was performed demonstrating the efficacy of intravesical oxybutynin compared to oral administration in adult patients. This study found a significant increase in bladder capacity and a significant decrease in side effects in the intravesical oxybutynin group. Due to the relative difficulties of intravesical oxybutynin delivery (preparation, cost) and the more invasive nature, it is not used as an alternative to oral oxybutynin.

The hypothesis of this study is that this treatment may have a legitimate place in the treatment of neurogenic bladder in patients with failure of anticholinergic treatment before a therapeutic escalation requiring an invasive procedure (Botox®, enterocystoplasty) especially in children for whom repeated general anesthesia for Botox® injection may interfere with brain development. In this way, the investigators aim to extend the time to therapeutic escalation in the pediatric population.

The main objective of the trial is to compare the efficacy on maximal bladder capacity of intravesical oxybutynin instillation versus placebo in the treatment of children with overactive neurogenic bladder (spina bifida), performing intermittent catheterization, for whom oral anticholinergic treatment is ineffective or poorly tolerated.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Person affiliated to or beneficiary of a social security plan

In failure of treatment with one or more anticholinergics defined by a response considered insufficient by the investigator after at least 4 weeks of optimal dose treatment, unable to take oral oxybutynin or intolerable adverse events

Having performed renal ultrasonography less than 2 months ago

Having performed cystomanometry less than 6 months ago including maximal bladder capacity and maximal bladder pressure (preferably not under oral oxybutynin treatment)

Disqualifiers

Person displaying known allergy to one of the components of evaluated product (notably oxybutynin).

Person with congestive cardiac failure

Person with cardiac arrhythmia

Person with tachycardia

Trial design

Design model

Parallel

Treatments tested in this trial

  • Oxybutynin Hydrochloride

    Drug

    Pharmaceutical form: solution. Route of administration: Intravesical. Medicinal product unique ID: PRD8074745. EU active substance code: SUB03581MIG.

  • Placebo

    Drug

    Pharmaceutical form: solution. Route of administration: Intravesical.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: IntraVesical Oxybutynin (IVO)Experimental treatment 1 intervention
Group B: IntraVesical Placebo (PCB)Placebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Evolution of maximal bladder capacity at 4 weeks of treatment (end of follow-up)

This parameter is considered by experts to be an objective marker of improvement in neurological bladder, in addition to the secondary clinical objective. It was used as the primary objective in the only prospective study in the literature. It is obtained by cystomanometry and is defined by the maximum volume (in mL) measured at the moment when permission to urinate is given to the patient, after filling via urethral catheter. In younger patients, urination occurs spontaneously, and this value is obtained a posteriori by curve analysis. If treatment is successful, maximum bladder capacity should increase.

Time frame
4 weeks

Secondary outcomes

1

Evolution of maximal bladder pressure at 4 weeks of treatment (end of follow-up)

This parameter is considered by experts to be an objective marker of neurological bladder improvement, in addition to the primary objective. This data is obtained during cystomanometry. If treatment is effective, it should decrease.

Time frame
4 weeks
2

Urinary incontinence

Time to clinical treatment failure defined by criteria found in literature and marketing authorization of Botox® in a 28-day time frame (at least one of the 3 criteria): * Treatment judged as non-effective by either the patient or the practitioner; * Reduction of urinary incontinence to less than 50% of the initial occurrences measured in the initial bladder diary; * Intolerable side effects reported by the patient.

Time frame
4 weeks
3

Evaluation of the number of side effects

Side effects are recorded by the patient in a treatment follow-up booklet or by the practitioner during follow-up. They include digestive, psychiatric, neurological, cutaneous and urological disorders, pain associated with instillation of the product, and other effects.

Time frame
4 weeks
4

Proportion of responders at 4 weeks of treatment

This corresponds to patients who achieved at least a 50% reduction in urinary incontinence episodes after 4 weeks of treatment, with no intolerable side effects (leading to discontinuation of treatment) at the end of the study. The number of incontinence episodes are collected over 72 consecutive hours in the week preceding each visit (V1, V2 and V3) by the patient on a bladder diary. Side effects are recorded by the patient in the treatment follow-up booklet and by the practitioner at each visit.

Time frame
4 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Central Hospital, Nancy, France

Lead sponsor

Ministry of Health, France

Collaborator

FARCO PHARMA

Collaborator