- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05968352
Restoration of Bladder Function in Spinal Cord Injury
The aim of this study is to develop improved methods of restoring function to the neurogenic bladder, using electrical stimulation without cutting nerves in patients with spinal cord injury.
The investigators will test 5-10 subjects with existing sacral anterior root stimulation (SARS) devices and look at the effects of high frequency (up to 600Hz) compared to the usual low frequency stimulation on bladder function. The investigators are particularly interested in whether it is possible to reproduce a 'functional' dorzal rhizotomy using high frequency stimulation of the S2 efferent nerves
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a proof of concept study of the effects on the urinary bladder and sphincter of high frequency stimuli applied to sacral efferent nerves. The effects on the bladder of low frequency stimuli applied to sacral afferent nerves will also be studied. It is also part of an academic collaboration between Oxford and Stanford University. The results will not be sold to Stanford but will be shared to enhance the development of therapies for patients with spinal cord injury. There is no intention to commercialise the findings at this stage nor to use the data for CE-marking.
Participants will be patients with clinically complete spinal cord injury who already have a commercially available implanted Finetech Brindley bladder stimulator with electrodes on the sacral nerves or roots, controlled by an external transmitter whose frequency can be adjusted by the investigator. This study will explore modified stimulation parameters and will deliver the stimulation pattern with a modified/experimental external stimulation control unit. The motivation for exploring these parameters is to see if clinical efficacy might be improved for future systems.
Primary outcome: Measurement of the effects of high and low frequency stimulation of the sacral efferent nerves on Bladder Pressure, rectal pressure, Detrusor pressure, Sphincter pressure, volume voided, post-void residual volume, voiding flow rate
Secondary measures: Effects of low frequency stimulation on bladder pressure, bladder capacity and reflex incontinence
The exploration of these novel stimulation parameters will require modification of the existing CE-marked system. The modifications will be limited to the external stimulation control unit, and will not compromise either the implantable system or its capability to continue normal operation with the existing CE-marked external control unit. The modified external stimulation control unit will be referred to as the "research stimulation controller." The use environment for the research stimulation controller will be a controlled hospital/laboratory setting, under clinical supervision. Outside of the clinic, the CE-marked system will be used to ensure normal therapy is provided to the subject. Access to the research stimulation controller will be controlled by the PI to prevent inadvertent misuse.
The development of the research stimulation controller will follow accepted good design practices. More specifically, the team will use a scaled version of 13845-compliant processes to 1) assess user needs 2) generate a risk analysis and plan 3) develop system requirements from design inputs 4) document and summarize design outputs 5) perform device verification tests and 6) perform user validation tests. These files will be maintained in a controlled document system.
The modified controller is similar to the CE marked device but will allow the investigators to explore a wider range of electrical stimulation parameters such as different waveforms and higher frequencies. Our intention is to use up to 600 Hz frequencies, compared to the existing frequencies in this device of up to 53 Hz. These changes are modest and are well within the energy delivery provided by existing commercial neuromodulation systems such as spinal cord stimulation (typical parameters for spinal cord stimulation include the Nevro® system that delivers up to 10kHz). Patients both with and without posterior sacral rhizotomy will also be included. No further surgery is required. Measurements of bladder function will be made in the urodynamic laboratory.
The study is prospective and unblinded. Each participant will serve as their own control; outcome measures will be compared with different frequencies of electrical stimuli and with no electrical stimuli.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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-
Oxon
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Oxford, Oxon, United Kingdom, OX3 9DU
- Recruiting
- University of Oxford
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Contact:
- Alexander L Green, PhD
- Phone Number: +44(0)1865234762
- Email: alex.green@nds.ox.ac.uk
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Contact:
- Alex Fung, MB BS
- Email: alex.fung1@nhs.net
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with clinically complete spinal cord injury who have undergone implantation of a Finetech Brindley Bladder controller, with or without sacral posterior rhizotomy.
- Male or female, aged 18 years or over.
- Patients willing and able to give informed consent to involvement in the study
Exclusion Criteria:
- External urethral sphincterotomy
- Patients are taking part in any studies on drugs or devices that alter bladder or autonomic function
- Any other significant comorbidity or illness that would preclude their participation or increase the risk to them of participating in the study
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Bladder Pressure
Time Frame: 2-3 hours
|
Urodynamics testing - High frequency SARS
|
2-3 hours
|
Rectal Pressure
Time Frame: 2-3 hours
|
Urodynamics- High frequency SARS
|
2-3 hours
|
Detrusor Pressure
Time Frame: 2-3 hours
|
Urodynamics- High frequency SARS
|
2-3 hours
|
Sphincter Pressure
Time Frame: 2-3 hours
|
Urodynamics1- High frequency SARS
|
2-3 hours
|
Volume voided
Time Frame: 2-3 hours
|
urodynamics- High frequency SARS
|
2-3 hours
|
Post-void residual volume
Time Frame: 2-3 hours
|
Urodynamics- High frequency SARS
|
2-3 hours
|
Voiding Flow Rate
Time Frame: 2-3 hours
|
Urodynamics- High frequency SARS
|
2-3 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Bladder pressure
Time Frame: 2-3 hours
|
Urodynamics - Low frequency SARS
|
2-3 hours
|
Bladder Capacity
Time Frame: 2-3 hours
|
Urodynamics - Low frequency SARS
|
2-3 hours
|
Reflex incontinence
Time Frame: 2-3 hours
|
Urodynamics - Low frequency SARS
|
2-3 hours
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRAS 260021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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