ClinicalTrials.Veeva

Menu

Single-incision Sling vs Urethral Bulking During Prolapse Surgery for Occult Stress Incontinence

T

The Christ Hospital

Status

Completed

Conditions

Stress Incontinence, Female

Treatments

Drug: Bulkamid bulking agent
Device: Single incision sling

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries

Full description

The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries. Charts will be reviewed for patients who had single- incision sling or urethral bulking injection with other prolapse surgeries to address occult stress incontinence at The Christ Hospital from the period of January 2019 to June 2021. Patients who didn't have any occult stress incontinence pre-operatively and didn't receive any anti-incontinence procedure during their prolapse surgery will be included as a control group. Surgical details, adverse events and postoperative voiding times will be collected from the chart. Patients will be contacted by a telephone to administer a validated questionnaire; a 3-day bladder diary to quantify urinary incontinence will be send to the patient to complete and return by mail.

The purpose of the study is to investigate whether urethral bulking is as effective as single- incision sling in treating occult stress incontinence.

Enrollment

60 patients

Sex

Female

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • -Females who are 18 years or old who were scheduled to either urethral bulking (Bulkamid) or single-incision sling (Altis sling) to address occult SUI with prolapse surgery. All patients reported no history of SUI preoperatively and during office physical exam, positive SUI was demonstrated during prolapse reduction.
  • Females who are 18 years or old who didn't have occult stress incontinence before their prolapse surgery and didn't receive any stress incontinence surgery during their prolapse surgery during the same period will be included as a control group.
  • English speaking patients.

Exclusion criteria

  • Patients who had either single-incision sling or urethral bulking with documented preoperative history of stress incontinence. Patients with a history of previous surgery for SUI.

Trial design

60 participants in 2 patient groups

Single incision sling group
Description:
The patient will receive Altis mini-incision sling for treatment of occult SUI
Treatment:
Device: Single incision sling
Urethral bulking group
Description:
The patient will receive Bulkamid urethral bulking agent for treatment of SUI
Treatment:
Drug: Bulkamid bulking agent

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems