Columbus, OHNCT07692789Now EnrollingIRB Ready

Pelvic Organ Prolapse Clinical Trial in Columbus, OH

Access cutting-edge pelvic organ prolapse treatment through this clinical trial at a research site in Columbus. Study-provided care at no cost to qualified participants.

Sponsored by Ohio State University

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Expert Care in Columbus

Access pelvic organ prolapse specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related pelvic organ prolapse treatment provided free

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Check if you qualify for this pelvic organ prolapse clinical trial in Columbus, 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 Columbus

    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 Columbus site if eligible
  4. 4Begin participation

About This Pelvic Organ Prolapse Study in Columbus

The purpose of this study is to evaluate the impact of pre-procedure patient reminder systems on patient satisfaction, preparedness, and anxiety among patients undergoing urodynamics studies. The rate of successful procedure completion will be compared between a prospective intervention group and a historical control group to determine whether the intervention improves procedural success and healthcare delivery.

Sponsor: Ohio State University

Who Can Participate

Inclusion Criteria

Age 18 years or older
Sex assigned at birth: Female.
English-speaking
Scheduled to undergo a urodynamics study at the OSU Upper Arlington Outpatient Clinic, OSU New Albany Outpatient Clinic, or OSU Eye and Ear Institute
Ability to access a telephone
Active MyChart account
Ability to provide informed consent
Documented post-residual volume of less than 150 mL
Ability to be reached by telephone after three call attempts
Negative point-of-care urinary tract infection on the day of the scheduled procedure (SOC)

Exclusion Criteria

Under 18 years of age
Patients with structural causes of urinary retention/incomplete bladder emptying (defined as a post-void residual \>150ml) or a positive point-of-care urinary tract infection on the day of the procedure.
Men are excluded as the population of interest is the female urogynecology population in both urology and obstetrics and gynecology.
Patients without access to a telephone or an active MyChart account are excluded because the intervention relies on telephone calls and electronic messaging for delivery of pre-procedure education and reminders.
Individuals who cannot be reached by telephone are excluded because they cannot receive the intervention.
Non-English speaking individuals are excluded because they will not be able to receive the standardized phone call in English and will not be able to complete the informed consent.

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 Columbus?

Yes, this clinical trial (NCT07692789) has an active research site in Columbus, 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.

Pelvic Organ Prolapse Treatment Options in Columbus, OH

If you're searching for pelvic organ prolapse treatment options in Columbus, OH, this clinical trial (NCT07692789) 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 Columbus research site is actively enrolling participants for this clinical trial. You'll receive care from experienced pelvic organ prolapse 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 pelvic organ prolapse clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Columbus, OH