West Columbia, SCNCT07247136Now EnrollingIRB Ready

Urinary Urge Incontinence Clinical Trial in West Columbia, SC

Access cutting-edge urinary urge incontinence treatment through this clinical trial at a research site in West Columbia. Study-provided care at no cost to qualified participants.

Sponsored by Neuspera Medical, Inc.

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Expert Care in West Columbia

Access urinary urge incontinence specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related urinary urge incontinence treatment provided free

Apply for This West Columbia Location

Check if you qualify for this urinary urge incontinence clinical trial in West Columbia, SC

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to West Columbia

    Convenient for SC residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit West Columbia site if eligible
  4. 4Begin participation

About This Urinary Urge Incontinence Study in West Columbia

Single-arm study conducted in participants for the treatment of urinary urge incontinence in patients who have failed, could not tolerate, or were not a candidate for more conservative treatments. The objective of the study is to assess the effectiveness of 30-minutes daily therapeutic stimulation with the Neuspera System.

Sponsor: Neuspera Medical, Inc.

Who Can Participate

Inclusion Criteria

Is male or female 22 years of age or older.
Has a diagnosis of UUI for greater than or equal to 6 months prior to the screening baseline visit date.
Has failed, could not tolerate (stopped taking medication due to lack of efficacy or intolerable side effects), or not a good candidate for (as determined by treating physician) at least one (1) antimuscarinic or β3 adrenoceptor agonist medication.
Is willing and able to washout (at least five half-lives) from OAB medications for a period determined appropriate based on type of OAB medication prior to the baseline bladder diary and remain off OAB medications through the study duration OR must be willing to maintain medication through the study duration.
Has a diagnosis of UUI with at least 4 UUI episodes on a 72-hour diary.
Has a positive stimulation trial with a 50% reduction in UUI episodes.

Exclusion Criteria

Has a contraindication for the Neuspera SNM System per the device labeling.
Has a hemoglobin A1c of \>8%.
Has glucosuria.
Has diabetic neuropathy.
Has interstitial cystitis or bladder pain syndrome as defined by either American Urological Association (AUA) or European Association of Urology (EAU) guidelines, chronic pelvic pain, or recurrent symptomatic urinary tract infections.
Has skin, orthopedic, neurological, or hematological (bleeding disorder) or anatomical limitations that could prevent successful placement of the neurostimulator.
Has broken, blistered skin or compromised circulation in the area of the neurostimulator implant.
Has neurogenic bladder dysfunction such as traumatic or atraumatic myelopathy, multiple sclerosis, Parkinsonism, or history of cerebrovascular accident.
Has documented urinary retention within 6 months prior to the screening baseline visit date.
Has clinically significant bladder outlet obstruction.
Is currently undergoing or has previously undergone pelvic irradiation.
Is a subject with a mechanical obstruction such as benign prostatic hypertrophy, urethral stricture, or cancer.
Has current grade 3 or 4 pelvic organ prolapse including cystocele, rectocele, enterocele, procidentia or vaginal vault prolapse.
Has received tibial nerve stimulation (TNS) in the past 3 months for the treatment of overactive bladder or unwilling to stay off TNS therapy for the study duration.
Has received treatment of urinary symptoms with any botulinum neurotoxin type-A (BoNT-A) agent in the past 6 months; (e.g. obotulinumtoxinA, Botox,® abobotulinumtoxinA, Dysport® IncobotulinumtoxinA, Xeomin®).
Is a woman who is pregnant or planning to become pregnant during this clinical study or is a woman of child-bearing potential who is not using a medically acceptable method of birth control. Women of child-bearing potential must undergo a pregnancy test, with clear negative result.
Has previously had SNM therapy.
Has active implantable medical devices such as neurostimulators, drug pumps, pacemakers, or internal defibrillators since compatibility has not been assessed.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in West Columbia?

Yes, this clinical trial (NCT07247136) has an active research site in West Columbia, SC that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Urinary Urge Incontinence Treatment Options in West Columbia, SC

If you're searching for urinary urge incontinence treatment options in West Columbia, SC, this clinical trial (NCT07247136) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our West Columbia research site is actively enrolling participants for this clinical trial. You'll receive care from experienced urinary urge incontinence specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all urinary urge incontinence clinical trials near you to find additional studies recruiting in your area.

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