Cincinnati, OHNCT06843538Now EnrollingIRB Ready

Postoperative Urinary Retention (POUR) Clinical Trial in Cincinnati, OH

Access cutting-edge postoperative urinary retention (pour) treatment through this phase 3 clinical trial at a research site in Cincinnati. Study-provided care at no cost to qualified participants.

Sponsored by TriHealth Inc.

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Expert Care in Cincinnati

Access postoperative urinary retention (pour) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related postoperative urinary retention (pour) treatment provided free

Apply for This Cincinnati Location

Check if you qualify for this postoperative urinary retention (pour) clinical trial in Cincinnati, OH

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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 Cincinnati

    Convenient for OH 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 Cincinnati site if eligible
  4. 4Begin participation

About This Postoperative Urinary Retention (POUR) Study in Cincinnati

The purpose of this research study is to determine if taking tamsulosin preoperatively decreases your chances of being discharged after surgery with a Foley catheter (flexible tube that drains urine from the bladder into a collection bag).

Sponsor: TriHealth Inc.

Who Can Participate

Inclusion Criteria

\- Patients undergoing any pelvic organ prolapse repair or incontinence surgery

Exclusion Criteria

Any surgery involving a non-urogynecologist
Patients already on an alpha blocker
Baseline hypotension
History of syncope
Postural orthostatic tachycardia syndrome (POTS)
Non-English speaker or interpreter unavailable for Spanish-speaking patient
Impaired cognition impeding proper consenting
Any other medical contraindication for tamsulosin use
History of urinary retention requiring continuous or intermittent catheterization
Patients consented for the study but then due to intraoperative complication, routine voiding trial no longer indicated due to requiring indwelling catheter or intermittent catheterization on discharge will be excluded from primary outcome analysis

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 Cincinnati?

Yes, this clinical trial (NCT06843538) has an active research site in Cincinnati, OH 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.

Postoperative Urinary Retention (POUR) Treatment Options in Cincinnati, OH

If you're searching for postoperative urinary retention (pour) treatment options in Cincinnati, OH, this clinical trial (NCT06843538) 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 Cincinnati research site is actively enrolling participants for this phase 3 clinical trial. You'll receive care from experienced postoperative urinary retention (pour) 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 postoperative urinary retention (pour) clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Cincinnati, OH