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Stress Incontinence, Female clinical trials

View clinical trials related to Stress Incontinence, Female.

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NCT ID: NCT06369922 Not yet recruiting - Pain Clinical Trials

TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence.

TENSUB
Start date: July 1, 2024
Phase: N/A
Study type: Interventional

This will be a double-blind randomized control trial in women with stress urinary incontinence who are undergoing an outpatient transurethral bulking procedure for stress urinary incontinence. Subjects will be identified by the University of Rochester urologists and urogynecologists participating in the study who currently oversee stress incontinence care. Subjects will be randomized into two groups. One group will be undergoing the cystoscopy with transcutaneous electrical nerve stimulation (TENS) for analgesia, and the second group will have the cystoscopy with placebo TENS.

NCT ID: NCT06232525 Recruiting - Clinical trials for Stress Incontinence, Female

A Randomized Comparison of Transobturator Tape With the Plication of Urethral Ligaments in the Treatment of Stress Urinary Incontinence

added
Start date: January 2, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the efficacy of transobturator tape (TOT) operation and urethral ligament plication operation in stress incontinence patients. The main question: - Which operation is more effective in treatment of stress incontinence? - Which operation has less complication and risks? Participants will be followed about 5 days, 2.5 months, 6 months and 1 year after the operation and asked about the continence status and complications.

NCT ID: NCT06012370 Not yet recruiting - Clinical trials for Stress Incontinence, Female

Injecting Plasma-rich Platelets & Hyaluronic Acid for Patients With Stress Urinary Incontinence

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

Injection of PRP and hyaluronic acid in stress incontinence patients

NCT ID: NCT05858125 Recruiting - Clinical trials for Urinary Incontinence

Social Media Navigation Aid Kits for Urinary Incontinence

SNAK
Start date: April 24, 2023
Phase: N/A
Study type: Interventional

This study aims to compare the effectiveness of a Urogynecology Social Media Navigation Aid Kit (SNAK) and routine counseling in the treatment of women with newly diagnosed urinary incontinence. The study will conduct a randomized controlled trial on treatment-naïve patients seeking care for urinary incontinence. The research will have five aims: 1. evaluate the impact of SNAK on patients' self-efficacy in managing urinary incontinence symptoms 2. compare patient satisfaction with urinary incontinence treatment between SNAK and routine counseling groups 3. assess the impact of SNAK on urinary incontinence severity 4. evaluate the impact of SNAK on patients' quality of life 5. examine if there is an impact of SNAK on patients' treatment decision. Participants will be randomized to routine counseling alone versus routine counseling plus a SNAK. They will be given a baseline survey at their initial enrollment to the study. The investigators will follow up at a 3-month interval where they will be given a post-intervention survey.

NCT ID: NCT05768607 Recruiting - Clinical trials for Stress Incontinence, Female

Laparoscopic Extraperitoneal ( Modified) Burch Colposuspension

Start date: January 17, 2023
Phase: N/A
Study type: Interventional

Urinary incontinence is a very common problem in women and can be seen at any age. Laparoscopic burch operation has been shown to be an effective, convenient and safe method in women with stress incontinence. Laparoscopic Burch operation is less invasive because it is advantageous in terms of hospitalization time, blood loss, pain and recovery time, but the disadvantage is the procedure time. Modified extraperitoneal technique may be a good method for lowering the procedure time.

NCT ID: NCT05210738 Completed - Clinical trials for Stress Incontinence, Female

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

Start date: January 1, 2019
Phase:
Study type: Observational

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

NCT ID: NCT04136652 Completed - Laser Clinical Trials

Vaginal CO2 Laser for Stress Incontinence

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Our aim with this study is to determine if transvaginal CO2 laser- treatment (DEKA SmartXide2 Laser System, MonaLisa Touch), renders significant effect in women with SUI. To best test this hypothesis, the study will be performed in a prospective, randomised controlled fashion in our institution. We will measure the effect as patient reported improvement using a validated scale (ICIQ-UI SF) as well as an objective measurement (stress test)

NCT ID: NCT03866356 Completed - Nursing Clinical Trials

The Effectiveness of a Stress Incontinence Care Protocol

SICP
Start date: December 1, 2016
Phase: N/A
Study type: Interventional

This study seeks to contribute to nursing practices by developing and stress incontinence care protocol with the help of the Star model and implementing this care protocol for the purpose of standardizing patient care outcomes.

NCT ID: NCT03847922 Terminated - Pain Clinical Trials

Nitrous Oxide for Analgesia During Office Urethral Bulking

Start date: February 15, 2019
Phase: Phase 4
Study type: Interventional

This study is designed to determine primarily if there is a difference in perceived pain in patients receiving urethral bulking with calcium hydroxylapatite using local lidocaine versus local lidocaine plus nitrous oxide gas. Patients will be randomized to a control group (local lidocaine plus room air) or a intervention group (local lidocaine plus 50% nitrous oxide/50% oxygen inhaled mixture). Their pain will be assessed immediately after the procedure, and their recollection of pain will also be assessed at their 2 week post-procedure visit. There are other secondary outcome measures as well; please see outcome measures section for full description.

NCT ID: NCT03672461 Completed - Clinical trials for Urinary Incontinence, Stress

A Group-Based Therapeutic Yoga Intervention for Urinary Incontinence in Ambulatory Older Women

Start date: March 6, 2019
Phase: N/A
Study type: Interventional

The investigators will conduct a randomized controlled trial to evaluate the efficacy of a group-based yoga intervention to decrease the frequency and impact of urinary incontinence in ambulatory middle-aged and older women and explore potential mediators of improvement in outcomes. Women aged 45 years and older who report daily or more frequent stress-, urgency-, or mixed-type incontinence, are not already engaged in formal yoga or muscle stretching/strengthening programs, are willing to temporarily forgo other clinical treatments for incontinence, are able to walk to and use the bathroom without assistance, and meet other eligibility criteria will be recruited from multiple locations surrounding the San Francisco Bay area.