Ignite Creation Date:
2024-05-06 @ 8:15 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06314412
Status:
RECRUITING
Last Update Posted:
2024-03-18
First Post:
2024-03-04
Brief Title:
Transcutaneous Posterior Tibial Nerve Stimulation in Patients With Multiple Sclerosis Related Urge Incontinence
Sponsor:
Istituto Auxologico Italiano
Organization:
Istituto Auxologico Italiano
Study Overview
Official Title:
Perineal Rehabilitation Efficacy of Transcutaneous Posterior Tibial Nerve Stimulation in Patients With Multiple Sclerosis Related Urge Incontinence
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
SANS-REHAB
Brief Summary:
Recently several studies have investigated the safety and efficacy of the Stoller afferent nerve stimulation SANS treatment in Multiple Sclerosis MS patients However because of the differences among the published protocols percutaneous versus transcutaneous stimulation stimulation site total number of sessions and the absence of data on the duration of the effect this treatment is not yet currently included in the rehabilitation programs The present study aims at evaluating the efficacy of a protocol of SANS in the short- and medium-term follow-up
The efficacy of the proposed stimulation protocol on the physiological parameters of bladder function will be also investigated
The efficacy of the proposed stimulation protocol on the physiological parameters of bladder function will be also investigated
Detailed Description:
The primary outcome will be the variation of urinary urgency and incontinence It will be evaluated by self-reported measuring scales such as the Overactive Bladder Questionnaire OAB-q and the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form ICIQ-UI SF in their Italian forms
The expected outcome is that the treatment of posterior tibial nerve stimulation will reduce the frequency and the urgency of urination and urinary incontinence Moreover results from the follow-up will allow estimating the duration of the expected outcome
The expected outcome is that the treatment of posterior tibial nerve stimulation will reduce the frequency and the urgency of urination and urinary incontinence Moreover results from the follow-up will allow estimating the duration of the expected outcome
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None