Electrical Stimulation for Continence After Spinal Cord Injury

NCT ID: NCT02978638

Last Updated: 2025-08-03

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-09-30
• Study Completion Date: 2025-09-28

Brief Summary

This study aims to improve continence and voiding of patients with spinal cord injury using electrical stimulation.

The Finetech Vocare Bladder System is an implantable sacral nerve stimulator for improving bladder and bowel function in patients with spinal cord injury (SCI). It has been commercially available in Britain and other countries since 1982, and has been used in thousands of patients with SCI to improve bladder, bowel and sexual function. It received FDA approval in 1998 under Humanitarian Device Exemption H980005 and H980008 for providing urination on demand and to aid in bowel evacuation.

Electrical stimulation to produce bladder contraction and improve bladder voiding after spinal cord injury has usually been combined with cutting of sensory nerves to reduce reflex contraction of the bladder, which improves continence. However, cutting these nerves has undesirable side effects. This study will not cut any sensory nerve. This study is testing the use of the stimulator for inhibiting bladder contraction by stimulating sensory nerves to improve continence after spinal cord injury, and for blocking sphincter contraction to improve voiding.

Detailed Description

Human subjects will be recruited from people with clinically complete spinal cord injury.

Subjects who meet the selection criteria described below will be screened to identify those whose reflex bladder contractions are inhibited by neuromodulation using low levels of electrical stimulation via electrodes on the skin over the dorsal genital nerve. Serial filling cystometries will be performed in the clinical urodynamic laboratories at the study sites. Bladder capacity and compliance will be recorded for each cytometrogram. Subjects whose reflex bladder contractions are significantly inhibited by this neuromodulation will be offered enrollment in the trial. Subjects whose reflex bladder contractions are not significantly inhibited by this neuromodulation, or who do not wish to participate in the study, will be able to continue with their usual form of bladder management.

After screening, selected subjects will be offered surgical implantation of a Vocare Bladder System in the FDA-approved manner, but without posterior rhizotomy. Because posterior rhizotomy is not performed, the afferent axons in the sacral nerves are intact and can be stimulated after surgery via the electrodes connected to the implanted stimulator.

The Vocare Bladder System will be implanted in the FDA-approved manner but without posterior rhizotomy.

After implantation, subjects will be evaluated in the urodynamic laboratory. Stimulation will applied to S34 sacral nerves bilaterally, and the effects on bladder capacity and continence and voiding will be measured.

Continence of urine will be documented by bladder diaries. These diaries will be completed initially as an inpatient in the SCI Service and then at home while applying neuromodulation via the implant.

It is expected that sacral neuromodulation by this method will be associated with a significant increase in bladder capacity and continence.

It is possible that this neuromodulation will not be associated with an increase in bladder capacity or continence. If so, subjects will still be able to use conventional methods of managing continence and should have no loss of function.

Participants whose bladder capacity and continence are improved by neuromodulation using the implanted stimulator will be offered the opportunity to continue to use the stimulator for the duration of the study and will be reviewed at three-month intervals. At the end of the study they will be reviewed again with their usual clinician and if there are no contra-indications to continued use of the stimulator will be offered the opportunity to continue its use under continued clinical follow-up from their usual clinician.

Participants whose bladder capacity and continence are not improved by neuromodulation using the implanted stimulator, or who do not wish to continue using the implanted stimulator, will be reviewed with their usual clinician and offered the bladder management they were using prior to the study. The implanted stimulator will be switched off, but will not be removed unless the participant wishes it to be removed or the investigators or the participant's usual clinician consider it in the participant's interest to be removed. It is usually simpler and safer for the participant to leave the stimulator implanted but inactive.

All participants will be provided with appropriate documentation regarding safety and electromagnetic compatibility of the device.

The investigation is justified because the potential benefits are greater than the potential risks, as follows:

The potential benefit of the research to the subjects are:

1. Improved bladder capacity

2. Improved continence

The potential benefits of the research to others are:

Evidence that bladder capacity and continence after spinal cord injury can be improved by electrical stimulation without cutting nerves.

The risks to subjects are reasonable in relation to the anticipated benefits to subjects and others because of

1. The high prevalence and severity of clinical complications caused by bladder complications after spinal cord injury

2. The paucity of methods of restoring continence after spinal cord injury that are safe, effective and without undesirable side effects

This study is primarily aimed at demonstrating safety, feasibility and proof of concept. It may also produce statistically and clinically significant evidence of efficacy that can be used to plan future clinical trials.

Significance:

If the technique of reducing reflex bladder contraction by implanted stimulation of the S34 nerve bilaterally is successful, it will open the door to more effective use of neuromodulation for continence after spinal cord injury.

Conditions

Spinal Cord Injury; Neurogenic Bladder; Incontinence

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Finetech Vocare Bladder System

This is a pilot study of the Finetech Vocare Bladder System to improve continence and voiding in human subjects with chronic spinal cord injury. Each subject will act as their own control, comparing function with the Finetech Vocare Bladder System in use and not in use.

Group Type: OTHER

Finetech Vocare Bladder System

Intervention Type: DEVICE

Participants will be implanted with the existing FDA-approved Finetech Vocare Bladder System stimulator and electrodes.

Interventions

Finetech Vocare Bladder System

Participants will be implanted with the existing FDA-approved Finetech Vocare Bladder System stimulator and electrodes.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

Subjects will be included if they meet all of the following criteria:

• Complete spinal cord injury (AIS grade A) of at least 2 years duration with neurological level (ISNCSCI level) below C4
• Impaired bladder emptying due to Detrusor External Sphincter Dyssynergia-DESD (unco-ordinated contraction of bladder and external urethral sphincter) as shown on video-urodynamic testing.
• Impaired continence due to detrusor hyper-reflexia

Exclusion Criteria

Subjects will be excluded if they meet any of the following criteria:

• Absence of reflex contractions of the bladder as shown on urodynamic testing
• Absence of reflex contractions of the external urethral sphincter as shown on urodynamic testing with EMG
• External sphincterotomy, urethral stricture or previous urethral or sphincter or bladder or prostate surgery
• History of pelvic fracture
• Subjects on anticoagulants or with coagulation disorders
• Immunosuppressed subjects
• Active or recurrent pressure ulcers, particularly in sacral, ischial or trochanteric areas
• Active untreated infection
• Active implanted medical device such as cardiac pacemaker or defibrillator
• Progressive spinal cord injury
• Pregnancy
• Mechanical ventilator dependency
• Any other significant co-morbidity or illness that would preclude their participation or increase the risk to them of participating in the study
• Inability or unwillingness to follow study protocol or give informed consent

• Minimum Eligible Age: 22 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

VA Palo Alto Health Care System

FED

Sponsor Role: collaborator

Stanford University

OTHER

Sponsor Role: collaborator

Case Western Reserve University

OTHER

Sponsor Role: collaborator

Santa Clara Valley Medical Center

OTHER

Sponsor Role: collaborator

University of New Mexico

OTHER

Sponsor Role: collaborator

Palo Alto Veterans Institute for Research

OTHER

Sponsor Role: lead

Responsible Party

Graham Creasey

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Graham H. Creasey, MD

Role: PRINCIPAL_INVESTIGATOR

Palo Alto Veterans Institute for Research

Reza Ehsanian, MD PhD

Role: STUDY_DIRECTOR

University of New Mexico

Locations

Palo Alto Veterans Institute for Research

Palo Alto, California, United States

Santa Clara Valley Medical Center

San Jose, California, United States

University of New Mexico

Albuquerque, New Mexico, United States

MetroHealth Medical Center

Cleveland, Ohio, United States

Countries

United States

References

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Reference Type: BACKGROUND

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Reference Type: BACKGROUND

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Reference Type: BACKGROUND

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Reference Type: BACKGROUND

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Reference Type: BACKGROUND

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Reference Type: BACKGROUND

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Other Identifiers

W81XWH-14-2-0132

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

CRE0004AGG

Identifier Type: -

Identifier Source: org_study_id