Non-Invasive combo therapy aims to restore bladder function in spinal cord injury

NCT ID NCT07704268

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time

Summary

This trial investigates whether combining high-frequency magnetic stimulation of the sacral nerve roots with ultrasound therapy to the bladder can reduce involuntary bladder contractions in people with spinal cord injury. Participants receive daily treatments for three weeks, and researchers measure changes in bladder capacity and wall elasticity. The goal is to find a non-invasive way to improve bladder control and reduce complications.

What this could mean

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

Active substance
a combination of high-frequency magnetic stimulation and ultrasound therapy applied to the sacral nerve roots and bladder
What this could lead to
If successful, this approach could offer a non-invasive way to improve bladder control and quality of life for people with spinal cord injury.
What could go wrong
This is a small, early-stage trial with only 44 participants, so results may not apply to everyone. The treatment is also time-intensive, requiring daily sessions for three weeks.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 44 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

An estimate. End dates often move.

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.

Ages

18 to 80 years

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: 1. Diagnosis of spinal cord injury (SCI) above the sacral level according to the International Standards for Neurological Classification of Spinal Cord Injury (revised 2011), confirmed by CT or MRI; 2. Detrusor overactivity confirmed by urodynamic study; 3. No severe urinary system diseases such as tumors, stones, infection, or organic urinary tract obstruction; 4. No severe hepatic/renal insufficiency, pulmonary, or cardiovascular diseases; 5. Aged 18-80 years; 6. Able to understand and comply with the required examinations, rehabilitation assessments, and treatment, and provide written informed consent. Exclusion Criteria: 1. Unstable vital signs or critically ill condition; 2. Severe autonomic dysreflexia; 3. Presence of metallic implants within 10 cm of the magnetic stimulation treatment area; 4. Any other diseases or conditions that may interfere with the study outcomes.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • Rehabilitation Center of Shengjing Hospital, China Medical University, shenyang, Liaoning 110000

    Shenyang, China

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