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Treatment of Neurogenic Detrusor Overactivity: Early Versus Late Pudendal Nerve Stimulation in Spinal Cord Injury (SCI) Patients

Primary Purpose

Neurogenic Detrusor Overactivity, Spinal Cord Injury

Status
Withdrawn
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
external electric pudendal nerve stimulation
Sponsored by
Ulrich Mehnert
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neurogenic Detrusor Overactivity focused on measuring neurogenic detrusor overactivity, neuromodulation, spinal cord injury, pudendal nerve stimulation, videocystometry, neurophysiology, neuroplasticity

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Single event traumatic or ischemic Para- or Tetraplegia
  • Complete SCI (ASIA A)
  • Lesion level between C4 and Th10
  • Performance of study treatment and assessments possible according to the study time schedule
  • Patient capable and willing of giving written informed consent

Exclusion Criteria:

  • Nontraumatic Para- or Tetraplegia (i.e. disc herniation, tumor, AV- Malformation, myelitis) exkl. single event ischemic incidences
  • Pre- known dementia or severe reduction of intelligence, leading to reduced capabilities of cooperation or giving consent
  • Peripheral Nerve lesions below the level of lesion (i.e. pudendal nerve impairment, cauda equina syndrome, pre- known Polyneuropathy)
  • Severe craniocerebral injury
  • Previous or planned intradetrusor injections of botulinum toxin
  • Previous or planned surgical therapy for neurogenic detrusor overactivity (e.g. bladder augmentation, Mitrofanoff, sphincter prothesis, sacral neuromodulation, deafferentation, sphincterotomy)

Sites / Locations

  • Guttmann Institute
  • Schweizerisches Paraplegikerzentrum Nottwil
  • Balgrist University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Early pudendal stimulation

Late pudendal stimulation

Control

Arm Description

Subjects in this arm will start with the intervention within 2 weeks after SCI

Subjects in this arm will start with the intervention 12 weeks after SCI

Subjects in this arm will be treated according to standard therapy but will receive no pudendal stimulation

Outcomes

Primary Outcome Measures

Videocystometry

Secondary Outcome Measures

Neurophysiological measurements (NCV, BCR, SSR)

Full Information

First Posted
January 6, 2010
Last Updated
July 19, 2019
Sponsor
Ulrich Mehnert
Collaborators
Institut Guttmann, Schweizerisches Paraplegikerzentrum Nottwil, BG Unfallklinik Murnau, Klinik für Paraplegiologie, Universitätsklinikum Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT01043848
Brief Title
Treatment of Neurogenic Detrusor Overactivity: Early Versus Late Pudendal Nerve Stimulation in Spinal Cord Injury (SCI) Patients
Official Title
Therapeutic Effects of Early and Late Onset Peripheral Pudendal Neurostimulation on Bladder Function and Autonomic Neuroplasticity in SCI - a Controlled European Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Withdrawn
Why Stopped
Poor patient recruitment, necessary number of patients could not be included within the required time frame
Study Start Date
December 2009 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ulrich Mehnert
Collaborators
Institut Guttmann, Schweizerisches Paraplegikerzentrum Nottwil, BG Unfallklinik Murnau, Klinik für Paraplegiologie, Universitätsklinikum Heidelberg

4. Oversight

5. Study Description

Brief Summary
Background: Although a small group, special attention has to be given to lower urinary tract (LUT) dysfunctions in spinal cord injury (SCI) patients, as they also suffer under a loss of motor-sensory function and autonomic regulation next to the severe deficiencies in bladder and bowel control. Autonomic dysregulation linked with LUT dysfunction can cause autonomic dysreflexia with life threatening increases in blood pressure and there is still no concept for an early rehabilitation of bladder function after SCI. Hypothesis: We assume that inadequate reorganization of nerve fibres in SCI is a reason for spastic bladder dysfunction and vegetative dysregulation and that this can be positively influenced by early neuromodulation. We hypothesized that bladder dysfunction as well as autonomic dysreflexia will be positively affected. Specific aims: Evaluation, if external pudendal nerve stimulation (EPS) can positively influence LUT rehabilitation in SCI patients and if early initiation of stimulation is more effective compared to late initiation (after spinal shock). Experimental design: Prospective multicentre study in 36 SCI patients (24 treatment subjects, 12 control subjects). EPS will be started either within 10 days after SCI (early stim group) or after cessation of spinal shock (late stim group). Effects on spastic bladder function and autonomic disinhibition will be assessed by urodynamics, vegetative tests, and by electrophysiological techniques. Expected value: If early EPS is effective and complete SCI patients benefit from this intervention; and if early onset of EPS has better and longer lasting effects than late onset stimulation, the findings will be of utmost relevance not only for bladder function but also to alleviate adverse phenomena such as autonomic dysreflexia. Neurostimulation may bear the opportunity to early reshape maladaptive neuroplasticity. This would be proof of an effective modulation and promotion of neuroplasticity, thus opening up new treatment options in the field of paraplegiology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurogenic Detrusor Overactivity, Spinal Cord Injury
Keywords
neurogenic detrusor overactivity, neuromodulation, spinal cord injury, pudendal nerve stimulation, videocystometry, neurophysiology, neuroplasticity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early pudendal stimulation
Arm Type
Experimental
Arm Description
Subjects in this arm will start with the intervention within 2 weeks after SCI
Arm Title
Late pudendal stimulation
Arm Type
Experimental
Arm Description
Subjects in this arm will start with the intervention 12 weeks after SCI
Arm Title
Control
Arm Type
No Intervention
Arm Description
Subjects in this arm will be treated according to standard therapy but will receive no pudendal stimulation
Intervention Type
Procedure
Intervention Name(s)
external electric pudendal nerve stimulation
Other Intervention Name(s)
contic+, tic Medizintechnik GmbH, 46286 Dorsten, Germany
Intervention Description
intervention timing: twice daily for 20 minutes during 3 consecutive months. intervention procedure: electrodes will be placed around the penile shaft (in males) or clips will be directly placed on the clitoris (in females). intervention device: contic+ stimulation parameters: 10 Hz, 200μs pulse width, 10mA (or less, if too uncomfortable).
Primary Outcome Measure Information:
Title
Videocystometry
Time Frame
week 4, 12, 26, 38, 52 after SCI
Secondary Outcome Measure Information:
Title
Neurophysiological measurements (NCV, BCR, SSR)
Time Frame
week 2, 4, 12, 26, 38, 52 after SCI

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Single event traumatic or ischemic Para- or Tetraplegia Complete SCI (ASIA A) Lesion level between C4 and Th10 Performance of study treatment and assessments possible according to the study time schedule Patient capable and willing of giving written informed consent Exclusion Criteria: Nontraumatic Para- or Tetraplegia (i.e. disc herniation, tumor, AV- Malformation, myelitis) exkl. single event ischemic incidences Pre- known dementia or severe reduction of intelligence, leading to reduced capabilities of cooperation or giving consent Peripheral Nerve lesions below the level of lesion (i.e. pudendal nerve impairment, cauda equina syndrome, pre- known Polyneuropathy) Severe craniocerebral injury Previous or planned intradetrusor injections of botulinum toxin Previous or planned surgical therapy for neurogenic detrusor overactivity (e.g. bladder augmentation, Mitrofanoff, sphincter prothesis, sacral neuromodulation, deafferentation, sphincterotomy)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ulrich Mehnert, MD
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martin Schubert, MD
Organizational Affiliation
Balgrist University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guttmann Institute
City
Badalona
State/Province
Barcelona
ZIP/Postal Code
08916
Country
Spain
Facility Name
Schweizerisches Paraplegikerzentrum Nottwil
City
Nottwil
State/Province
Luzern
ZIP/Postal Code
6207
Country
Switzerland
Facility Name
Balgrist University Hospital
City
Zurich
ZIP/Postal Code
8008
Country
Switzerland

12. IPD Sharing Statement

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Treatment of Neurogenic Detrusor Overactivity: Early Versus Late Pudendal Nerve Stimulation in Spinal Cord Injury (SCI) Patients

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