New London, CTNCT07215780Now EnrollingIRB Ready

Pelvic Organ Prolapse Clinical Trial in New London, CT

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

Sponsored by Yale University

Quick Self-Assessment

See if you qualify for this New London location

Preparing your pre-screening questions…

Expert Care in New London

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

Apply for This New London Location

Check if you qualify for this pelvic organ prolapse clinical trial in New London, CT

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to New London

    Convenient for CT 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 New London site if eligible
  4. 4Begin participation

About This Pelvic Organ Prolapse Study in New London

The purpose of this study is to evaluate the utility of postoperative sitz baths in patient pain perception and recovery following surgical repair of prolapse. The SORE Study is a prospective, randomized controlled trial that aims to compare postoperative pain intensity one week after native tissue repair of pelvic organ prolapse for patients undergoing a sitz bath regimen versus usual care. Findings from this study may contribute to more robust, multimodal postoperative pain management plans if proven efficacious or, alternatively, reduce plastic medical waste and simplify postoperative pain plans if found to be ineffective.

Sponsor: Yale University

Who Can Participate

Inclusion Criteria

Female ≥ 18 years of age at time of surgery
English or Spanish-speaking
Documentation of pelvic organ prolapse as evidenced by Stage 2, 3, or 4 prolapse on preoperative Pelvic Organ Prolapse Quantification system (POP-Q) examination
Surgery to be performed by a urogynecologist
Ambulatory or inpatient surgery acceptable

Exclusion Criteria

Mesh-augmented prolapse repair (robotic, laparoscopic, or open sacrocolpopexy or sacrohysteropexy, vaginal mesh)
Urogynecologic surgery without prolapse repair (i.e. midurethral sling, intravesicular botox, hysterectomy only)
Suspected genital herpes simplex virus (HSV), molluscum contagiosum virus (MCV), condyloma acuminata, or vulvar/vaginal skin and soft tissue infection at recruitment by patient report
Daily opioid use (short or long-acting)
Concurrent non-urogynecologic surgery (i.e. rectopexy, staging or debulking for malignancy)
Lack of access to operative report
Pregnant (as determined by positive urine pregnancy test on the day of surgery via standard testing or current pregnancy documented in the preoperative note)
Incarcerated
Unable to give consent/conserved
Unable to complete study intervention or assessment per investigators

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 New London?

Yes, this clinical trial (NCT07215780) has an active research site in New London, CT 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 New London, CT

If you're searching for pelvic organ prolapse treatment options in New London, CT, this clinical trial (NCT07215780) 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 New London 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.

More Pulmonary Embolism Trials in New London, CT

See all pulmonary embolism clinical trials recruiting in New London — not just this study.

Browse Pulmonary Embolism Trials in New London →

Browse More Trials by Condition

Pulmonary Embolism TrialsAntiphospholipid Syndrome TrialsInterstitial Cystitis TrialsGeographic Atrophy TrialsPelvic Floor Disorders TrialsAll Conditions →

Ready to Join in New London?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · New London, CT