Magnetic chair may help men regain bladder control faster after prostate surgery
NCT ID NCT07698028
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This study investigates whether adding a non-invasive magnetic stimulation treatment to standard pelvic floor exercises helps men recover bladder control more quickly after prostate surgery for an enlarged prostate. Participants who experience urine leakage after surgery will be randomly assigned to do pelvic floor exercises alone or exercises plus magnetic stimulation sessions using a specialized chair. Researchers will track how long it takes for bladder control to return, how much leakage occurs, and the impact on quality of life over six months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Extracorporeal Magnetic Stimulation (ExMI) via a specialized chair
- What this could lead to
- If it works, this could offer a non-invasive, drug-free way to speed up bladder control recovery after prostate surgery, improving quality of life.
- What could go wrong
- This is a relatively small, early-stage trial. The added benefit of magnetic stimulation over exercises alone may be modest, and results may not apply to all types of prostate surgery.
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
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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
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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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
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50 years and older
- Sex
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Male participants only
- Healthy volunteers
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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 Hide 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: * Male patients aged ≥50 years * Diagnosed with symptomatic benign prostatic hyperplasia (BPH) requiring surgical intervention * Scheduled for Holmium Laser Enucleation of the Prostate (HoLEP) or Bipolar Enucleation of the Prostate (BipoLEP) * Development of postoperative stress-predominant urinary incontinence after catheter removal * Presence of postoperative urinary leakage requiring at least one safety pad/day * Ability to understand and perform pelvic floor muscle training instructions * Ability and willingness to attend extracorporeal magnetic stimulation sessions and follow-up visits Exclusion Criteria: * Preoperative urinary incontinence or neurogenic bladder dysfunction * Previous prostate surgery or prior anti-incontinence surgery * Urethral stricture disease or bladder neck contracture * Active urinary tract infection at the time of enrollment * Severe cognitive impairment preventing compliance with PFMT instructions * Neurological disorders affecting lower urinary tract function, including Parkinson disease, multiple sclerosis, spinal cord injury, or cerebrovascular stroke with residual deficits * Implanted electronic or metallic devices contraindicating magnetic stimulation, including cardiac pacemaker, implantable cardioverter-defibrillator, neurostimulators, or cochlear implants * Uncontrolled diabetes mellitus with severe neuropathy * Receiving concurrent therapies for urinary incontinence during the study period * Persistent postoperative complications requiring reintervention (e.g., severe hematuria, clot retention) * Inability or refusal to complete follow-up evaluations
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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.
Contacts and locations
Locations
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Tanta University Hospital
Tanta, 31111, Egypt
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Other studies related to the condition(s) this trial covers.
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