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Urinary Incontinence, Stress clinical trials

View clinical trials related to Urinary Incontinence, Stress.

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NCT ID: NCT06021769 Recruiting - Clinical trials for Pelvic Organ Prolapse

Pessary Experience Study

Start date: June 12, 2023
Phase:
Study type: Observational

Pessaries are silicone devices inserted into the vagina for treatment of pelvic organ prolapse or stress urinary incontinence. They are adequate treatment options for patients who are poor surgical candidates, those who decline surgical intervention, or as a temporizing measure in those ultimately planning surgery. Most studies suggest that about 75% of patients are able to be successfully fit with a pessary, but about 50% discontinue pessary use within 12 months of initiation. The purpose of this study is to determine why pessaries are discontinued.

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: NCT05961241 Completed - Clinical trials for Urinary Stress Incontinence

Pelvic Floor Muscle Function Among Running Women

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

This study will examine pelvic floor muscles function amongst women who run on a regular basis compared to controls. Women who do not run, will begin running protocol, and second evaluation will be performed following 2 months of training. Urinary incontinence will also be assessed.

NCT ID: NCT05954234 Completed - Low Back Pain Clinical Trials

Combining Pelvic Floor Rehabilitation With Postural Re-education in Women With Stress Urinary Incontinence and Chronic Low Back Pain: a Preliminary Study.

Start date: April 20, 2021
Phase: N/A
Study type: Interventional

Stress Urinary incontinence (SUI) is a common health condition in female population. Although its prevalence increases with the age, women of all ages could be affected. Several epidemiological studies have shown an association of SUI with Low Back Pain (LBP) demonstrating, moreover, that the presence of one condition may predispose the patient to the onset of the other. Concerning the LBP, the clinical practice guidelines provided recommendations for physical rehabilitative treatment. Different techniques and physical exercises have been developed and it is difficult at the date to affirm the superiority of one approach as compared to another. Moreover, the crucial role plays by the pelvic floor muscles (PFM) both as an integral part of trunk and lumbo-pelvic stability and in maintenance of urinary continence, lead the pelvic floor muscles disfunction to be associated both with SUI and LBP, making the PFM rehabilitation a useful approach in both the conditions. In this rehabilitative context the present study aims to verify the effectiveness of a global physical approach based on postural re-education combined to the pelvic floor rehabilitation in women with diagnosis of stress urinary incontinence associated with non-specific chronic low back pain.

NCT ID: NCT05952258 Enrolling by invitation - Clinical trials for Stress Urinary Incontinence

Magnetic Stimulation as a Treatment for Stress Urinary Incontinence

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

The goal of this clinical trial is to determine the efficacy of electromagnetic stimulation treatment of the pelvic floor muscles in adult females with stress urinary incontinence.

NCT ID: NCT05948397 Not yet recruiting - Quality of Life Clinical Trials

To Use the Combined Version of ICIQ-SF and Quality of Life Scale in Mixed Urinary Incontinence

Start date: August 1, 2023
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is detecting the dominant component of mixed urinary incontinence via a combined version of ICIQ-SF and quality of life scale. The main question it aims to answer is: 1. Which component (urgency or stress) urinary incontinence bothers the patient more?

NCT ID: NCT05944484 Completed - Clinical trials for Stress Urinary Incontinence

Effect of Visceral vs Total Body Fat Reduction in Obese Female With Stress Urinary Incontinence

Start date: November 30, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the visceral fat reduction versus total body fat reduction on stress urinary incontinence in obese females.

NCT ID: NCT05912491 Completed - Clinical trials for Stress Urinary Incontinence

Transperineal Ultrasonography in Stress Urinary Incontinence

Start date: July 1, 2012
Phase:
Study type: Observational

Pelvic organ prolapse (POP) and urinary incontinence (UI) are common female disorders. Accurate diagnosis of the aetiology of pelvic organ descent and prolapse with or without accompanying urination disorders is essential for appropriate therapeutic management. Imaging and functional urodynamic testing are being increasingly used in the diagnosis of this pathology, because precise assessment of the damage to the supporting and ligament apparatus is essential for therapeutic success. Pelvic floor ultrasound can facilitate dynamic assessment of static changes that occur during functional tests. Such assessments can provide additional insights into existing defects, which have explorative value and allow for targeted correction of damage, and may thus indirectly contribute to reduced rates of revision surgeries.

NCT ID: NCT05900570 Recruiting - Clinical trials for Stress Urinary Incontinence

Effect of Peri-Urethral Stimulation on Intra-Urethral Pressure

Start date: February 26, 2024
Phase: N/A
Study type: Interventional

The purpose of this early feasibility prospective study is to gain initial understanding of the effect of acute peri-urethral neurostimulation on the perineal nerves on intra-urethral pressure.

NCT ID: NCT05892575 Not yet recruiting - Aging Clinical Trials

The Effect of Incontinence Program Applied to Obese Elderly on Quality of Life, Coping and Loneliness

Start date: July 2023
Phase: N/A
Study type: Interventional

The goal of this: It was planned in a single-blind randomized controlled pre-test-post-test experimental research design. The aim of this study is to determine the effect of urinary incontinence management program on quality of life, coping with incontinence and loneliness in obese elderly. The main questions it aims to answer are: Does the Urinary Incontinence Management Program prepared for the obese elderly affect the quality of life, coping with incontinence and loneliness levels of the elderly in the experimental and control groups? After the Urinary Incontinence Management Program prepared for the obese elderly, is there an increase in the incontinence quality of life of the obese elderly in the experimental group compared to the obese elderly in the control group? After the Urinary Incontinence Management Program prepared for the obese elderly, is there an increase in the level of coping with incontinence of the obese elderly in the experimental group compared to the obese elderly in the control group? After the Urinary Incontinence Management Program prepared for the obese elderly, is there a decrease in the loneliness levels of the obese elderly in the experimental group compared to the obese elderly in the control group? After the Urinary Incontinence Management Program prepared for the obese elderly, is there an increase in the incontinence quality of life, coping with incontinence and loneliness levels of the elderly in the experimental group after the intervention compared to the pre-intervention?