Wichita, KSNCT07209397Now EnrollingIRB Ready

Overactive Bladder Clinical Trial in Wichita, KS

Access cutting-edge overactive bladder treatment through this clinical trial at a research site in Wichita. Study-provided care at no cost to qualified participants.

Sponsored by InMode MD Ltd.

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Expert Care in Wichita

Access overactive bladder specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related overactive bladder treatment provided free

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Check if you qualify for this overactive bladder clinical trial in Wichita, KS

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Why Participate?

  • No-Cost Study Care

  • Local to Wichita

    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 Wichita site if eligible
  4. 4Begin participation

About This Overactive Bladder Study in Wichita

The goal of this clinical trial is to learn if a vaginal radiofrequency (RF) device called MORPHEUSV works to treat overactive bladder (OAB) in women. Researchers also want to learn how safe the device is for this indication. This study will include women ages 22 to 80 who have had OAB symptoms for at least 6 months. The main questions it aims to answer are: Does the MORPHEUSV device lower the number of daily episodes of accidental urine leakage caused by urgency? Does it work better than a sham (placebo) treatment? Researchers will compare the MORPHEUSV device to a sham treatment to see how well it reduces symptoms of overactive bladder. Participants will: 1) Receive one session of either the MORPHEUSV or sham treatment. 2) Track their symptoms using a diary and questionnaires 3) Return for three to six follow-up visits over 12 months. This study is being conducted at multiple clinics in the United States.

Sponsor: InMode MD Ltd.

Who Can Participate

Inclusion Criteria

Female, aged 22 to 80 years inclusive at the time of consent.
History of idiopathic overactive bladder (OAB) symptoms for ≥6 months.
At least 7 episodes of urge urinary incontinence (UUI) over 3 days, as recorded in a 3-day bladder diary during screening.
Urge-predominant incontinence, defined as greater number of UUI episodes than stress urinary incontinence (SUI) episodes during screening.
Willing and able to complete the 3-day bladder diary.
Willing to discontinue OAB medications (e.g., anticholinergics, beta-3 agonists) at least 2 weeks prior to baseline treatment visit, if currently taking such medications.
Willing to use a reliable method of contraception during the study period, if of childbearing potential and sexually active.
Negative pregnancy test at screening (if applicable).
Willing and able to provide written informed consent and comply with study procedures and follow-up schedule.

Exclusion Criteria

Predominant stress urinary incontinence (SUI) based on bladder diary
Currently pregnant, breastfeeding, or planning pregnancy during the study
History of neurologic conditions affecting bladder function (e.g., multiple sclerosis, spinal cord injury, Parkinson's disease)
Active urinary tract infection (UTI) at screening
History of interstitial cystitis, bladder pain syndrome, or chronic pelvic pain
Prior or current bladder cancer, pelvic malignancy, or pelvic radiation
Pelvic organ prolapse beyond the hymen (POP-Q stage \> II)
Implanted neuromodulation device or prior sacral nerve stimulation
Use of bulking agents, Botox, or surgical treatment for incontinence within 12 months
Prior pelvic floor RF treatment or laser vaginal rejuvenation
Significant pelvic anatomical abnormalities that interfere with treatment
Use of investigational drug or device within 30 days before screening
Any condition that, in the investigator's opinion, would interfere with safe study participation or data integrity
Uncontrolled systemic disease (e.g., uncontrolled diabetes, cardiovascular disease)
Inability or unwillingness to comply with study requirements or follow-up

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 Wichita?

Yes, this clinical trial (NCT07209397) has an active research site in Wichita, 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.

Overactive Bladder Treatment Options in Wichita, KS

If you're searching for overactive bladder treatment options in Wichita, KS, this clinical trial (NCT07209397) 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 Wichita research site is actively enrolling participants for this clinical trial. You'll receive care from experienced overactive bladder 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 overactive bladder clinical trials near you to find additional studies recruiting in your area.

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