Boulder, CONCT07485205Now EnrollingIRB Ready

Lower Urinary Tract Symptoms (LUTS) Clinical Trial in Boulder, CO

Access cutting-edge lower urinary tract symptoms (luts) treatment through this clinical trial at a research site in Boulder. Study-provided care at no cost to qualified participants.

Sponsored by Bright Uro

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Expert Care in Boulder

Access lower urinary tract symptoms (luts) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related lower urinary tract symptoms (luts) treatment provided free

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Check if you qualify for this lower urinary tract symptoms (luts) clinical trial in Boulder, CO

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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 Boulder

    Convenient for CO 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 Boulder site if eligible
  4. 4Begin participation

About This Lower Urinary Tract Symptoms (LUTS) Study in Boulder

A prospective, open-label, single arm interventional trial to establish normative reference ranges for urodynamics parameters in healthy adult participants using using the Glean Urodynamics System.

Sponsor: Bright Uro

Who Can Participate

Inclusion Criteria

Healthy male and female adults ages 18 to 45 years.
Patient is able to read, write, and communicate in English.
Patient is able to provide informed consent.
Patient owns, can independently operate, and is willing to use a smart device for study data collection purposes

Exclusion Criteria

Patient with any prior pregnancy (gravida ≥1), is currently pregnant (as confirmed by urine pregnancy test or medical history), or intends to become pregnant during the study period.
Patient has one or more symptoms indicative of a symptomatic 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 known history of urological conditions (e.g., recurrent UTIs, incontinence, symptomatic benign prostatic hyperplasia, neurogenic bladder, interstitial cystitis, urinary retention, any genitourinary cancer).
Patient has a known history of neurological conditions that can affect central nervous system function.
Patients with a current or prior diagnosis of diabetes mellitus (Type 1 or Type 2).
Patient is currently taking medications that may affect urological functions (e.g., diuretics, anticholinergics, alpha-blockers).
Patient has abnormal urinary habits if one or more of the following bladder events are reported on any day of the 3-day bladder diary: urinary frequency ≥ 8 times/day, ≥ 1 nocturia episode, ≥ 1 leak event, or ≥ 1 urgency event.
Patient has a total score on the Lower Urinary Tract Dysfunction Research Network Symptom Index-10 (LURN SI-10) questionnaire greater than 0; a total score of 1 is acceptable only if the sole positive response is urinary frequency of 4-7 times per day.
Patient has a urostomy and/or 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 would not be appropriate for this study as determined by the Principal Investigator.

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 Boulder?

Yes, this clinical trial (NCT07485205) has an active research site in Boulder, CO 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.

Lower Urinary Tract Symptoms (LUTS) Treatment Options in Boulder, CO

If you're searching for lower urinary tract symptoms (luts) treatment options in Boulder, CO, this clinical trial (NCT07485205) 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 Boulder research site is actively enrolling participants for this clinical trial. You'll receive care from experienced lower urinary tract symptoms (luts) 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 lower urinary tract symptoms (luts) clinical trials near you to find additional studies recruiting in your area.

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