Clinical trial · Interventional
Clinical Study of External Electrical Stimulation for Male Incontinence
Clinical Evaluation of Perineal Electrical Stimulation for Urinary Incontinence in Men
NCT06620419CI-TRIAL-00101712active not recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this research is to evaluate the effectiveness of the Elidah neuromuscular stimulation treatment to reduce incontinence in men post-prostatectomy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Urinary Incontinence | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Perineal-applied electrical stimulation | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment group
- description
- Self-applied electrical stimulation for 6 weeks.
- interventionNames
- Device: Perineal-applied electrical stimulation
Primary outcomes (1)
- measure
- Reduction in Leakage by Pad weight
- timeFrame
- 6 weeks
- description
- 24-hr pad weight
Secondary outcomes (6)
- measure
- Safety measured by no Adverse events
- timeFrame
- 6 weeks
- description
- No adverse events
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Scheduled for robotic-assisted laparoscopic prostatectomy * Read and speak English * Predominant SUI of at least 1 pad/day Exclusion Criteria: * History or symptoms of urinary incontinence, urinary retention, extra-urethral incontinence, overflow incontinence * Complete denervation of the pelvic floor * Severe Obesity as defined by BMI \>= 40 * Has undergone pre-op pelvic floor exercise strengthening * Pelvic pain/painful bladder syndrome * Implanted cardiac device, untreated cardiac arrhythmia or suffer from other heart problems. * History of epilepsy * Underlying neurologic/neuromuscular disorder * Metal implants in the abdomen or pelvic area * Chronic coughing * Impaired decision making, suicidal thoughts, or drug/alcohol dependence * Uncontrolled intercurrent illness that would limit compliance with study requirements * Lacks capacity to adhere with study requirements * Lacks capacity to consent for themselves.
References
Publications (0)
Data not yet available
No reference posted for this study.