Bethesda, MDNCT05221021Now EnrollingIRB Ready

Overactive Bladder Syndrome Clinical Trial in Bethesda, MD

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

Sponsored by Walter Reed National Military Medical Center

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Expert Care in Bethesda

Access overactive bladder syndrome specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related overactive bladder syndrome treatment provided free

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Check if you qualify for this overactive bladder syndrome clinical trial in Bethesda, MD

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Why Participate?

  • No-Cost Study Care

  • Local to Bethesda

    Convenient for MD 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 Bethesda site if eligible
  4. 4Begin participation

About This Overactive Bladder Syndrome Study in Bethesda

A single site, double-blinded, randomized controlled trial for postmenopausal women with urinary frequency, urgency, nocturia with or without urgency urinary incontinence symptoms. Patient's will be randomized between 0.01% vaginal estradiol cream with placebo oral pill or daily 50 milligrams oral Mirabegron with a placebo vaginal cream for 12 weeks.

Sponsor: Walter Reed National Military Medical Center

Who Can Participate

Inclusion Criteria

Raw score of 14 or more on OAB-q SF (adjusted score of 20)
Postmenopausal defined by not having a period for 12 months or bilateral oophorectomy a least 12 months status post procedure, or women with prior hysterectomy and preserved ovaries over age 55 years old or having a documented follicle stimulating hormone level greater than 40mIU/mL.
Ability to speak and read English

Exclusion Criteria

Contraindications to Vaginal Estrogen or Mirabegron
Post void residual \>200mL or \>1/3 patient's total bladder volume
Currently on or previously taking anticholinergic or beta- 3 agonists within the past 1 month
Symptomatic pelvic organ prolapse greater than Stage 2, contraindication to vaginal estrogen therapy
Undiagnosed postmenopausal vaginal bleeding within the past 12 months
Current diagnosis of Multiple sclerosis, Parkinson's Disease, prior spinal cord injury, Spina Bifida, prior pelvic irradiation, Interstitial Cystitis, recurrent urinary tract infection.

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 Bethesda?

Yes, this clinical trial (NCT05221021) has an active research site in Bethesda, MD 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 Syndrome Treatment Options in Bethesda, MD

If you're searching for overactive bladder syndrome treatment options in Bethesda, MD, this clinical trial (NCT05221021) 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 Bethesda research site is actively enrolling participants for this clinical trial. You'll receive care from experienced overactive bladder syndrome 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 syndrome clinical trials near you to find additional studies recruiting in your area.

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