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Urinary Incontinence, Stress clinical trials

View clinical trials related to Urinary Incontinence, Stress.

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NCT ID: NCT05771168 Recruiting - Clinical trials for Male Stress Urinary Incontinence

Surgery for Male Stress Urinary Incontinence

SMUI
Start date: September 29, 2022
Phase:
Study type: Observational [Patient Registry]

The purpose of this observational prospective study is to evaluate the success rate (cure plus improvement) of procedures for treatment of male stress urinary incontinence (artificial urinary sphincter or male slings) at 5 years of study follow-up and to determine other outcomes of surgical treatment for each of the devices and, to perform a prognostic factor analysis to identify clinical and surgical variables that correlate with (in)continence or revisions for each of the device subtypes. Cure is defined as urinary continence with no need for use of pads or the use of 1 light security pad; the improvement is defined as the reduction of≥ 50% of the number of pads with use of no more than two pads.

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: NCT05751213 Completed - Clinical trials for Urinary Incontinence,Stress

Knack Technique in Post-menopausal Women With Stress Urinary Incontinence

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

To determine the Effects of pelvic floor muscle exercise with and without Knack Technique in post-menopausal women with stress urinary incontinence

NCT ID: NCT05735223 Completed - Clinical trials for Prostate Adenocarcinoma

A Prospective Study to Evaluate the Impact of Maximal Urethral Length Preservation Technique During Robotic Laparoscopic Prostatectomy on the Stretched Flaccid Penile Length and Continence

Start date: September 30, 2021
Phase: N/A
Study type: Interventional

After robotic prostatectomy, besides erectile function and achievement of oncological control, staying dry is also a very important desire expressed frequently by the patients. This has led to the concept of trifecta achievement after robotic prostatectomies. Hence, continence preserving prostatectomies are the order of the day today. Patient acceptance to surgery is low if the continence cannot be assured preoperatively. Many techniques have been promulgated in the last two decades. The investigators present a novel technique of maximal urethral length preservation during surgery as an effective method of continence preservation. The investigators hypothesize that maximal preservation of urethra would lead to improved and early continence after robotic prostatectomy. The investigators also hypothesize that urethral preservation spares penile length shortening. The investigators therefore propose to prospectively evaluate penile length shortening. While penile length change after radical prostatectomy has been studied in the past, the investigators like to assess the penile morphometric assessment following the novel technique of maximal urethral length preservation radical prostatectomy.

NCT ID: NCT05733052 Recruiting - Clinical trials for Urinary Incontinence

Pubourethral Ligament Plication for the Surgical Treatment of Stress Urinary Incontinence

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

To test efficacy and safety at six months of the proposed Pubourethral Plication Procedure (PPP) for cure of stress urinary incontinence - reinforcing pubourethral ligaments (PUL) with large diameter polyester sutures.

NCT ID: NCT05732844 Completed - Clinical trials for Urinary Incontinence

Efficacy of the Use of Vaginal Balls for the Improvement of Urinary Incontinence and Sexual Function in Women.

Start date: October 5, 2022
Phase: N/A
Study type: Interventional

Asess if adding vaginal spheres treatment to the conventional Pelvic Floor Muscle Trainning (PFMT) produces a greater decrease in the severity of the stress urinary incontinence or a greater perceived quality of life related to incontinence.

NCT ID: NCT05721807 Completed - Clinical trials for Urinary Incontinence,Stress

Physiotherapy in Stress Urinary Incontinence

Start date: July 7, 2021
Phase: N/A
Study type: Interventional

The goal of this randomized controlled trial is to evaluate and compare the effects of functional magnetic stimulation and pelvic floor muscle training on pelvic floor muscle function, urinary incontinence symptoms and quality of life in women with stress urinary incontinence. The main questions it aims to answer are: - What is the effect of functional magnetic stimulation on pelvic floor muscle function, symptoms of urinary incontinence and quality of life in women with stress urinary incontinence? - What is the effect of pelvic floor muscle training program on pelvic floor muscle function, symptoms of urinary incontinence and quality of life in women with stress urinary incontinence? - Which intervention is more effective - functional magnetic stimulation or pelvic floor muscle training program? Participants will be evaluated before and after the intervention with the following methods: - International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF); - Incontinence Impact Questionnaire-Short Form (IIQ-7); - Pelvic floor muscle strength and endurance will be assessed with a "Pelvexiser" perineometer.

NCT ID: NCT05702827 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Use of a Dual-agent Local Analgesic (Bupivacaine-meloxicam) for Abdominal Incisions in Patients Undergoing Retropubic Mid-urethral Sling Surgery

Start date: January 23, 2023
Phase: Phase 3
Study type: Interventional

This study will compare the use of a dual-agent local analgesic (bupivacaine-meloxicam) for abdominal incisions in patients undergoing retropubic mid-urethral sling surgery to see if narcotic usage and pain are impacted.

NCT ID: NCT05702567 Completed - Clinical trials for Urinary Incontinence

The Effectiveness of Transvaginal Radiofrequency in Women With Stress Urinary Incontinence

Start date: January 9, 2023
Phase: N/A
Study type: Interventional

The following clinical trial investigates the efficacy of transvaginal radiofrequency in the physiotherapy treatment of stress urinary incontinence (SUI). The treatment compares transvaginal radiofrequency with pelvic floor muscle training (PFMT) and PFMT alone. The present study is a randomized controlled trial with double blinding (evaluator and patients). The objective is to evaluate what radiofrequency can provide in the improving of the quality of life, symptoms and pelvic floor muscle strength of patients with SUI. The reason for the combination with PFMT, is that it is the golden standard treatment in pelvic floor rehabilitation and SUI improvement.

NCT ID: NCT05693103 Recruiting - Clinical trials for Urinary Incontinence, Stress Incontinence

The Effect of High-Intensity Focused Electromagnetic on Urinary Incontinence Symptoms

Start date: August 15, 2021
Phase:
Study type: Observational [Patient Registry]

This study is aimed at women's pelvic floor muscles, especially urinary incontinence caused by pelvic floor muscle relaxation or pelvic prolapse, to observe whether the use of (HIFEM) high-intensity focused magnetic energy chairs can help the pelvic floor muscles after this treatment Strengthening to improve the symptoms of urinary incontinence caused by the compression of the sacral nerve plexus caused by the downward movement of the uterus, thereby improving the social life and quality of life of the patient.