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Urinary Incontinence, Stress clinical trials

View clinical trials related to Urinary Incontinence, Stress.

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NCT ID: NCT03942549 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Changes in the Bladder Micro-environment Following Midurethral Sling Surgery for Stress Urinary Incontinence

Start date: May 3, 2019
Phase:
Study type: Observational [Patient Registry]

This observational cohort study is aimed at determining changes in the cytokine expression profile as well as the urinary and vaginal microbiome of women undergoing midurethral sling placement for the treatment of stress urinary incontinence.

NCT ID: NCT03842410 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Solyx Single-Incision SlingDynamic Intraoperative Standing Sling Technique (DISST) as an Office-based Procedure

Start date: May 31, 2019
Phase: N/A
Study type: Interventional

This study will assess the feasibility and success of performing the SolyxTM SIMUS in the office using the Dynamic Interactive Standing Sling Technique (DISSTTM). Study endpoints will be feasibility, composite success, complications, and patient and physician acceptance.

NCT ID: NCT03681678 Active, not recruiting - Clinical trials for Urinary Incontinence

Laser Therapy for Treatment of Urogenital Symptoms in Women

Start date: October 8, 2018
Phase:
Study type: Observational [Patient Registry]

This is a prospective observational study of women undergoing vaginal treatment with the fractional carbon dioxide (fCO2) laser for various urogenital symptoms.

NCT ID: NCT03671694 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Laser Vaginal Treatment for SUI

Start date: September 19, 2018
Phase: N/A
Study type: Interventional

RCT designed to answer the question: Does the application of Erbium: YAG laser treatment to the vagina improve urine control for women with SUI?

NCT ID: NCT03620604 Active, not recruiting - Clinical trials for Urinary Incontinence,Stress

Mid Term Safety and Efficacy of ALTIS® Single Incision Sling for Female Stress Urinary Incontinence (SUI).

Start date: January 1, 2014
Phase:
Study type: Observational [Patient Registry]

Prospective, single-arm, non-sponsored, observational single centre trial in a cohort of patients undergoing stress urinary incontinence surgery with ALTIS® procedure. All patients were diagnosed according to clinical reports, physical exploration and urodynamics. Body mass index(BMI) was categorized according to World Health Organization classification. Valsalva leak point pressure was categorized in three groups <60 cmH2O, 60-90 cmH2O and >90 cmH2O). Participants were evaluated post-operatively at 1, 6, 12 and 24 months with physical examination, ICIQ-SF, visual scale of satisfaction(SVS)(0-10). Adverse events were reported in each visit. Multivariate analysis for risk factors of surgery failure was performed.

NCT ID: NCT03474653 Active, not recruiting - Clinical trials for Urinary Incontinence

LATITUDE An Observational Study of Patient Choice and the Urethral Bulking Agent, Bulkamid®

Start date: June 12, 2017
Phase:
Study type: Observational

Latitude is an observational study exploring how effective Bulkamid ® is as a first line treatment for women with stress urinary incontinence. Women who choose to have Bulkamid as part of their standard clinical care will be asked to complete questionnaires before and after their surgery so that we can assess how their urinary symptoms change. As a second part of the study, we are asking all patients having any first line treatment for stress incontinence to complete a short questionnaire telling us how they decided what treatment to have. A small number of these women will be contacted via telephone and asked whether they would mind being interviewed to tell us more about this. We will also interview a number of doctors taking part in Latitude to find out how they counsel patients about different treatment options for stress urinary incontinence.

NCT ID: NCT03203798 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Effects of Training of Pelvic Floor Muscles (MAP) on Stress Urinary Incontinence

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

In the current scientific literature, it is clear that SUI can cause several social, hygienic and personal relationship problems. It has also been proven that this condition affects many more menopausal women than menacme, and this is believed to be due to the hypoestrogenism characteristic of this phase. On the other hand, weakness of the pelvic floor muscles (PFM) is also related to the genesis of SUI. The role of these muscles would be to keep the bladder neck elevated (above the pubic symphysis) during increases in abdominal pressure, and its weakness would lead to excessive lowering of the bladder neck at these times, leading to SUI due to bladder neck hypermobility. The conservative treatment of this condition, therefore, encompasses the strengthening of PFMs, which would avoid excessive descent of the bladder neck during increases in abdominal pressure, thereby reducing urinary loss. In the current literature there are studies proving the effectiveness of pelvic floor muscle training; however, in relation to the literature on abdominal hipopressive gymnastics, it is observed that the scientific evidence is still poor, however, the technique is still Widely spread through extension courses offered throughout Latin America, France and Spain; With regard to the comparison of these methods with respect to their clinical efficacy and the quality of life and patient satisfaction, there are no consistent studies, and this fact motivated us to carry out this study.

NCT ID: NCT03120117 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Importance of Patient Positioning at Cough Test When Considering Success Following Sling Procedures

DISST
Start date: August 2013
Phase: N/A
Study type: Interventional

This is a prospective study to assess the feasibility and success of performing an intra-operative standing cough test and the correlation with the long term success of the sling surgery.

NCT ID: NCT03098992 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

The Efficacy and Safety of Fotona Smooth® Device for the Treatment of Stress Urinary Incontinence

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

There are many existing treatments of female stress urinary incontinence such as the use of adult absorbent pads and diapers, behavioral training, including bladder training, pelvic muscle exercises, biofeedback, urethral plugs, intravaginal prosthesis, electrical stimulation, periurethral injections, and reconstructive surgery. However, there is still a lack of effective minimally invasive treatment options that are independent of patient compliance. One emerging approach of minimally invasive SUI therapy is pelvic floor reinforcement using laser therapy. The primary objective of this post-marketing study is to confirm the effectiveness and safety of the FotonaSmooth® device in the treatment of stress urinary incontinence (SUI) in a large number of females using objective and subjective methods. Patients with stress incontinence will be assigned to two groups, an active group, where the Fotona Dynamis Er:YAG Laser System will be used, and a sham group where a very low laser setting will be used, and parameter presentations will be masked. Participants will be adult females, 18 years old and older with clinical and urodynamic diagnosis of Stress Urinary Incontinence,who have had no significant improvement in urinary incontinence from at least one previous conservative treatment, such as behavioral measures, pelvic floor muscle training or the use of absorbent pads

NCT ID: NCT03052985 Active, not recruiting - Clinical trials for Pelvic Organ Prolapse

Materiovigilance After Urinary Incontinence or Prolapse Surgery

VIGI-MESH
Start date: February 14, 2017
Phase:
Study type: Observational [Patient Registry]

Observatory of Materiovigilance After Surgery of Urinary Incontinence or Prolapse in Women Implantable medical devices (meshes) used in pelvic organ prolapse surgery (genital prolapse, rectal prolapse), or incontinence surgery may be source of severe complications.