Kansas City, KSNCT03767595Now EnrollingIRB Ready

Stress Urinary Incontinence Clinical Trial in Kansas City, KS

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

Sponsored by Uromedica

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Expert Care in Kansas City

Access stress urinary incontinence specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related stress urinary incontinence treatment provided free

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Check if you qualify for this stress urinary incontinence clinical trial in Kansas City, KS

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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 Kansas City

    Convenient for KS 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 Kansas City site if eligible
  4. 4Begin participation

About This Stress Urinary Incontinence Study in Kansas City

The ProACT Post Approval Study is a 5-year prospective, open-label, multi-center study designed to evaluate the long-term incidence of urethral stricture and device erosion after ProACT implantation. In addition, the study will evaluate whether treatment with ProACT affects clinical outcomes after subsequent SUI therapies.

Sponsor: Uromedica

Who Can Participate

Inclusion Criteria

Subject is a male of at least 50 years of age.
Subject demonstrates stress urinary incontinence.
Subject has undergone a radical prostatectomy, transurethral resection of the prostate, or other prostate surgery.
Subject is willing and able to undergo surgical implantation of ProACT devices.
Subject is willing and able to comply with study-required follow-up activities, including annual telephonic follow -up interviews, for a period of 5 years from their date of initial implantation. This includes compliance even after possible explant of ProACT devices and/or possible implantation of subsequent therapies.
Subject is willing and able to sign the approved informed consent.
Subject has two positive 24-hour pad weight tests (greater than or equal to 8 gram pad weight increase demonstrated in two 24-hour pad weight tests).
Subject has a negative urine culture.
Subject has no known urogenital malignancy, other than previously treated prostate cancer.
Subject meets ONE of the following criteria:
Baseline Prostate-Specific Antigen (PSA) of less than or equal to 2.5ng/mL;
Baseline PSA \> 2.5ng/mL and less than or equal to 10 ng/mL AND free PSA greater than or equal to 25% of total PSA;
Physician determines subject to be a suitable surgical candidate.

Exclusion Criteria

Subject has an existing urethral stricture, a history of any urethral strictures, or has ever had a urethrotomy.
Subject has undergone prostate surgery or any anti-incontinence surgery within the last 12 months.
Subject has an artificial urinary sphincter or any components of a previously implanted artificial urinary sphincter in vivo.
Subject has undergone radiation therapy in the prostatic area within the last 12 months.
Subject has untreated or unsuccessfully treated detrusor instability or over-activity.
Subject has an atonic bladder.
Subject had, presently has, or is suspected of having bladder cancer.
Subject has untreated or unsuccessfully treated bladder stones.
Subject has detrusor sphincter dyssynergia.
Subject has known hemophilia or a bleeding disorder.
Subject has a known severe contrast solution allergy (e.g., anaphylaxis, cardiac, or respiratory arrest).
Subject has insulin-dependent diabetes that is uncontrolled or not controllable, as indicated by an A1c test result of = 6.5%.

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 Kansas City?

Yes, this clinical trial (NCT03767595) has an active research site in Kansas City, KS 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.

Stress Urinary Incontinence Treatment Options in Kansas City, KS

If you're searching for stress urinary incontinence treatment options in Kansas City, KS, this clinical trial (NCT03767595) 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 Kansas City research site is actively enrolling participants for this clinical trial. You'll receive care from experienced stress urinary 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 stress urinary incontinence clinical trials near you to find additional studies recruiting in your area.

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