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Spinal cord injury bladder study pulled before it began

NCT ID NCT05968352

Knowledge-focused Sponsor: University of Oxford Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled This study
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aimed to test whether high-frequency electrical stimulation could improve bladder control in people with spinal cord injury who already have a special device implanted. Researchers planned to compare high-frequency versus low-frequency stimulation in 5 to 10 participants. However, the trial was withdrawn before enrolling anyone, so no data or conclusions are available.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Sacral Anterior Root Stimulation (SARS) device
What this could lead to
If successful, this could point toward a non-surgical way to improve bladder function and reduce incontinence in people with spinal cord injury.
What could go wrong
The trial was withdrawn before any participants were enrolled, so no results exist. It is a very small, early-stage study, and the approach may not work or may have unknown risks.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Started

Nov 2021

Finished

Oct 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients with clinically complete spinal cord injury who have undergone implantation of a Finetech Brindley Bladder Controller, with or without sacral posterior rhizotomy. John Radcliffe Hospital (Oxford), Royal National Orthopaedic Hospital (Stanmore) and Walton Centre (Liverpool) will be both patient identification centres and research sites for this study. Stoke Mandeville Hospital will be an additional patient identification centre, but studies on patients identified there will be conducted at Oxford as patients are generally under joint care between Stoke Mandeville Hospital and Oxford.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

spinal cord injury urinary bladder disorder urinary bladder, atony of

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Bladder dysfunction Spinal cord injuries

Contacts and locations

Locations

  • University of Oxford

    Oxford, Oxon, OX3 9DU, United Kingdom

More trials for these conditions

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