RECRUITING

Does Bladder Instillation Reduce Time to Discharge After Sling Surgery

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

The purpose of this randomized control trial study is to determine if intraoperative bladder instillation of fluid decreases the time to discharge after having an outpatient mid-urethral sling procedure, and to measure the cost savings of this decrease in hospital stay. Charges will be broken down between recovery room charges and discharge area, as recovery room charges are significantly higher. The investigators suspect that a shorter time in the recovery room will translate into fewer charges.

Official Title

Does Intraoperative Bladder Instillation Decrease Outpatient Recovery Time After Mid-Urethral Sling

Quick Facts

Study Start:2011-12
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02277288

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. 1. Female
  2. 2. Age 18 years or older
  3. 3. History of stress urinary incontinence
  4. 4. Scheduled for outpatient mid-urethral sling procedure, any approach
  1. 1. Age less than 18 years
  2. 2. Pregnancy
  3. 3. Inability to give informed consent
  4. 4. History of urinary retention

Contacts and Locations

Study Contact

Jennifer Anger, MD, MPH
CONTACT
3103852992

Principal Investigator

Jennifer Anger, MD, MPH
PRINCIPAL_INVESTIGATOR
Cedars-Sinai Medical Center

Study Locations (Sites)

Cedars-Sinai Medical Center
Beverly Hills, California, 90211
United States

Collaborators and Investigators

Sponsor: Cedars-Sinai Medical Center

  • Jennifer Anger, MD, MPH, PRINCIPAL_INVESTIGATOR, Cedars-Sinai Medical Center

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 Date2011-12
Study Completion Date2025-12

Study Record Updates

Study Start Date2011-12
Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

  • Stress Urinary Incontinence