Optimal Stimulation Rates in Sacral Neuromodulation Therapy

Completed

• Conditions: incontinence; overactive bladder; urinary retention; 10004994

• Registration Number: NL-OMON31616
• Lead Sponsor: Academisch Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 54

Inclusion Criteria

Patients with Sacral Neuromodulation therapy for complaints of urge incontinence, urgency frequency, hypocontractile detrusor or obstruction due to urethral sphincter overactivity.

Exclusion Criteria

Patients with Sacral Neuromodulation Therapy for other reasons than mentioned in the inclusion criteria

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Improvement in voiding diaries results between the *standard* frequency (10 Hz)<br /><br>and pulsewidth (210µs) and new settings. Improvement is measured by computer<br /><br>assisted comparison of voiding diaries taken with the *standard* settings and<br /><br>with the new settings and is reflected in percentage improvement achieved</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>* Patient toleration of rate changes.<br /><br>* Difference between optimal settings between patients with either urge<br /><br>symptoms or retention symptoms.</p><br>