Owings Mills, MDNCT07425015Now EnrollingIRB Ready

Urology Clinical Trial in Owings Mills, MD

Access cutting-edge urology treatment through this clinical trial at a research site in Owings Mills. Study-provided care at no cost to qualified participants.

Sponsored by Bright Uro

Quick Self-Assessment

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Expert Care in Owings Mills

Access urology specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related urology treatment provided free

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Check if you qualify for this urology clinical trial in Owings Mills, MD

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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 Owings Mills

    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 Owings Mills site if eligible
  4. 4Begin participation

About This Urology Study in Owings Mills

A prospective, open-label, single arm interventional trial evaluating the safety and performance of the in-clinic and extended monitoring of the lower urinary tract using the Glean Urodynamics System.

Sponsor: Bright Uro

Who Can Participate

Inclusion Criteria

Male or female patient must be ≥ 22 years of age.
Patient is a candidate for UDS per standard of care.
Patient is able to provide informed consent.

Exclusion Criteria

Patient has one or more symptoms indicative of a urinary tract infection (UTI) (i.e., fever, costovertebral angle pain or tenderness, suprapubic tenderness, worsening urinary frequency, worsening urgency, and/or dysuria).
Patient has a history of recurrent UTIs (≥ 3 episodes in previous 12 months).
Patient has used antibiotics within the past 7 days from the baseline/screening visit.
Patient diagnosed with neurogenic LUTD (i.e., one or more of these conditions: normal-pressure hydrocephalus, cerebral palsy, spinal cord injuries, traumatic brain injury, stroke, Parkinson's disease, multiple sclerosis, meningomyelocele, spina bifida, dementia, Guillain-Barre syndrome, and tumors involving the central nervous systems or spine).
Patient diagnosed with interstitial cystitis (IC), bladder pain syndrome, painful bladder syndrome or any etiology of chronic pelvic pain syndrome (CPPS).
Patient with a urostomy.
Patient with a colostomy.
Patient has an atypical anatomic structural variation or has had a previous surgical intervention that has permanently changed structural anatomy anywhere along their lower urinary tract (urethra, pelvic floor, urethral sphincter, and/or bladder wall) that the principal investigator deems might compromise the placement or retention of the Glean sensors during the study (e.g., strictures).
Patient has a Pelvic Organ Prolapse Quantification (POP-Q) of Grade III or higher (i.e., most distal portion of the prolapse protrudes more than 1 centimeter below the hymen).
Patient with any abnormal or concerning rectal conditions such as ongoing anal fissures, rectocele, fistula, active herpes, or active yeast infections.
Patient has a known inability to void.
Patient has a previous history of radiation leading to bleeding (e.g., hemorrhagic radiation cystitis).
Patient is pregnant (as confirmed by urine pregnancy test or medical history) or breastfeeding, pregnant within the past 6 months, or intending to become pregnant during the study period.
Patients who may not be able to independently use a smart device.
Subjects who, at the principal investigator's determination, would not be appropriate for this study.

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 Owings Mills?

Yes, this clinical trial (NCT07425015) has an active research site in Owings Mills, 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.

Urology Treatment Options in Owings Mills, MD

If you're searching for urology treatment options in Owings Mills, MD, this clinical trial (NCT07425015) 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 Owings Mills research site is actively enrolling participants for this clinical trial. You'll receive care from experienced urology 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.

Ready to Join in Owings Mills?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Owings Mills, MD