RECRUITING

Sequence of Midurethral Sling Placement During Robotic Sacrocolpopexy

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study looks at the best time to place a midurethral sling (MUS), which is a small piece of mesh used to treat stress urinary incontinence (SUI) (leaking urine when you cough, laugh, or exercise). The sling is placed during a type of surgery called robotic sacrocolpopexy (RSC). This surgery helps fix pelvic organ prolapse, when organs like the bladder or uterus drop from their normal place. Doctors can place the sling either before or after they lift and support the top of the vagina during surgery, but they aren't sure which timing works better. In this study, investigators are comparing what is the best time to place the sling, how the patient feels after surgery and if a patient's symptoms got better or worse.

Official Title

Sequence of Midurethral Sling Placement During Robotic Sacrocolpopexy

Quick Facts

Study Start:2025-07
Study Completion:2027-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07008898

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * At least 18 years of age
  2. * Able to speak and read English and Spanish
  3. * Diagnosis of pelvic organ prolapse stage 2-4
  4. * Planning to undergo a robotic-assisted sacrocolpopexy
  5. * Demonstrable SUI (either by CST, with or without prolapse reduction, or UDS) within the year prior to enrollment
  6. * Planning to undergo concomitant SUI correction with MUS at the time of RSC
  1. * Less than 18 years of age
  2. * Unable to speak and read English or Spanish
  3. * No diagnosis of SUI (prophylactic slings)
  4. * History of prior surgery for SUI
  5. * Bladder capacity \<200 mL or post-void residual (PVR) \>150 mL
  6. * Current genitourinary fistula or urethral diverticulum

Contacts and Locations

Study Contact

Martha K Coghlan, MD
CONTACT
6019883613
mkcoghlan@uabmc.edu
Gabriela E Halder, MD, MPH
CONTACT
205-975-0304
gehalder@uabmc.edu

Principal Investigator

Gabriela E Halder, MD, MPH
PRINCIPAL_INVESTIGATOR
University of Alabama at Birmingham

Study Locations (Sites)

University of Alabama at Birmingham
Birmingham, Alabama, 35233
United States

Collaborators and Investigators

Sponsor: University of Alabama at Birmingham

  • Gabriela E Halder, MD, MPH, PRINCIPAL_INVESTIGATOR, University of Alabama at Birmingham

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-07
Study Completion Date2027-06

Study Record Updates

Study Start Date2025-07
Study Completion Date2027-06

Terms related to this study

Keywords Provided by Researchers

  • Stress incontinence
  • Pelvic organ prolapse
  • Midurethral sling
  • Sucess rates
  • Complication rates
  • Patient satisfaction

Additional Relevant MeSH Terms

  • Stress Incontinence Female
  • Pelvic Organ Prolapse