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Sacral Neuromodulation & Urodynamics

Assessment of Predictive Role of Urodynamics in Sacral Neuromodulation Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03614767
Enrollment
100
Registered
2018-08-03
Start date
2017-08-01
Completion date
2022-07-31
Last updated
2019-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-obstructive Urinary Retention, Overactive Bladder

Brief summary

In the field of urology, sacral neuromodulation (SNM) is a well-accepted, second-line, minimally invasive treatment for patients with overactive bladder dry (OABD) or wet (OABW), and for patients with non-obstructive urinary retention (NOUR). Long-term vary between 50-60%. This study examines whether urodynamics can be used as a predictor for successful SNM therapy

Interventions

DIAGNOSTIC_TESTurodynamics

Bladder filling and pressure is measured by the insertion of probes within the bladder, urethra and anorectum.

Sponsors

Universiteit Antwerpen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Overactive bladder * Non-obstructive urinary retention

Exclusion criteria

* Neurogenica disorder (e.g. cerebrovascular accident, spinal cord injury)

Design outcomes

Primary

MeasureTime frameDescription
Change in bladder volume3 weeksChange in bladder volume is measured before and after test procedure for sacral neuromodulation
Change in bladder sensation3 weeksBladder sensation is measured by a slider (indicating bladder fullness scaled from 0 to 100) before and after test procedure for sacral neuromodulation
Change in ice water test3 weeksIce water is infused in the bladder and incontinence upon insertion of the ice water is assessed before and after sacral neuromodulation

Countries

Belgium

Contacts

Primary ContactStefan De Wachter, MD PhD FEBU
stefan.dewachter@antwerpen.be8215934

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026