Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05861011
Other study ID # ULora
Secondary ID 2023PI004
Status Completed
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date February 28, 2023

Study information

Verified date May 2023
Source University of Lorraine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Surgical outcomes of bladder neck surgery in children with neurogenic bladder. Consequences on bladder voiding.


Description:

Surgical outcomes of bladder neck surgery in children with neurogenic bladder: Quality of voiding: spontaneous, need for catheterization, or incontinence. Other surgical complications.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date February 28, 2023
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group N/A to 17 Years
Eligibility Inclusion Criteria: - Patients, with neurogenic bladder and younger than 18 years old ,who underwent a bladder neck procedure Exclusion Criteria: - Patients, with neurogenic bladder and older than 18 years old ,who underwent a bladder neck procedure

Study Design


Locations

Country Name City State
France ULorraine VandÅ“uvre-lès-Nancy Grand-Est

Sponsors (1)

Lead Sponsor Collaborator
University of Lorraine

Country where clinical trial is conducted

France, 

References & Publications (1)

Stein R, Bogaert G, Dogan HS, Hoen L, Kocvara R, Nijman RJM, Quaedackers J, Rawashdeh YF, Silay MS, Tekgul S, Radmayr C. EAU/ESPU guidelines on the management of neurogenic bladder in children and adolescent part II operative management. Neurourol Urodyn. 2020 Feb;39(2):498-506. doi: 10.1002/nau.24248. Epub 2019 Dec 3. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with delayed or incomplete opening of the bladder neck during the voiding phase of micturition impeding urine flow Cysto-urethrogram and uroflowmetry help diagnose delayed or incomplete opening of the bladder neck.
delayed or incomplete opening of the bladder neck
Baseline (Before surgery)
Primary Number of participants with muscular bladder The muscular bladder has thicker walls, bladder diverticula and trabecules (diagnosed during abdominal ultrasound, urethro-cystogram and cystoscopy) Baseline (Before surgery)
Secondary Length of stay Length of stay From admission to discharge home, up to 20 days
Secondary The time length between the surgery date and the postoperative consultation date Follow_up represents the time length between the surgery date and the postoperative consultation date in days, months, or years. Generally, there are a-month-follow-up, a three month-follow-up, a six month-follow-up, and a year-follow-up. The surgeon can see the patient if there is any problem between these consultations. After a year of follow-up, it is up to the surgeon to decide if the patient needs to be seen yearly or not. The last follow-up date is crucial because it indicates how the patient is and if other follow-up dates need to be applied. Through study completion, an average of 2 years
Secondary Surgical complications after bladder neck procedure bleeding, bowel obstruction, surgical hernia, urinary stone, urinary infection Through study completion, an average of 2 years
Secondary Operating time Operating time Intraoperative
See also
  Status Clinical Trial Phase
Recruiting NCT02978638 - Electrical Stimulation for Continence After Spinal Cord Injury N/A
Enrolling by invitation NCT06429631 - The Effect of CIC Education on QOL and Compliance With Mobile Application in Individuals With Spinal Cord Injury. N/A
Completed NCT03573726 - Use of a Diurnal Indwelling Urethral Catheter to Improve Quality of Life N/A
Recruiting NCT06059066 - Optimization of OnabotulinumtoxinA (BTX-A) Injection for the Treatment of Neurogenic Lower Urinary Tract Dysfunction N/A
Completed NCT01429090 - Bioavailability of Vagantin® Coated Tablets Relative to an Oral Methantheline Bromide Solution Phase 1
Recruiting NCT05587101 - Neurogenic Lower Urinary Tract Symptoms in Patients With Multiple Sclerosis
Terminated NCT03843073 - Connected Catheter- Safety and Effectiveness Study N/A
Terminated NCT04059159 - Connected Catheter - Safety and Effectiveness Study N/A
Completed NCT05858840 - Urinary Artificial Sphincter in Children
Completed NCT05861024 - Urinary Calculi After Bladder Augmentation in Children
Completed NCT04074616 - Reducing Anticholinergic Bladder Medication Use in Spinal Cord Injury With Home Neuromodulation N/A
Completed NCT05683938 - GentleCathâ„¢ Air Intermittent Catheter Smartwatch Real Life Pilot Study
Completed NCT04543552 - A Comparative Analysis of Portable Bladder Scanner to Determine Age/ Volume Specific Accuracy in 0-6 Years of Children
Active, not recruiting NCT06247033 - Efficacies of Different Managements in Patients With Overactive Bladder With Stroke N/A
Withdrawn NCT01305681 - Bacterial Properties With LoFric® Catheters During Clean Intermittent Catheterization Phase 1/Phase 2
Recruiting NCT04248322 - Qualitative Assessment of the Impact of TTNS on QOL and Participation
Recruiting NCT05301335 - Spinal COrd NeuromodulaTor by SpIneX and ScoNE to Treat NeurogeniC BladdEr - SCONE "CONTINENCE" Clinical Study N/A
Recruiting NCT04924569 - Continence Care Registry
Completed NCT01716624 - Botox Versus Oxybutynin as First Line Treatment for the Poorly Compliant Pediatric Neurogenic Bladder Phase 3
Completed NCT01297647 - Incidence of Urinary Tract Infection After Urodynamic Investigation N/A