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Active clinical trials for "Urinary Incontinence, Stress"

Results 31-40 of 519

Urinary Stress Incontinence and Urgency in Women With EMSELLA

Stress Urinary IncontinenceUrge Incontinence

The purpose of this prospective study is to examine the safety and efficacy of high intensity focused electromagnetic (HIFEM) technology for the treatment of women with stress urinary incontinence (SUI), urge incontinence (UI) and mixed stress urinary and urge incontinence (MUI), looking at any potential sexual health benefits that may be concomitantly achieved from this treatment.

Recruiting28 enrollment criteria

Adjustable Continence Therapy (ACT) for the Treatment of Female SUI

Urinary IncontinenceUrinary Incontinence,Stress

A prospective, single arm, non-randomized, multicenter, prospective case-series trial. The purpose of this trial is to demonstrate the safety and effectiveness of using the Adjustable Continence Therapy (ACT) to provide a clinically relevant improvement in stress urinary incontinence.

Recruiting26 enrollment criteria

Platelet Rich Plasma in Women With Urinary Incontinence

Urinary IncontinenceStress Urinary Incontinence

Stress urinary incontinence (SUI) is defined as involuntary loss of urine on effort or physical exertion or on sneezing or coughing. Platelet-rich plasma (PRP) is an autologous solution of human plasma containing various growth factors witch enhance regeneration and healing process. The aim of this study is to evaluate the efficacy and safety of PRP in the treatment of the female SUI.

Recruiting8 enrollment criteria

Pubourethral Ligament Plication for the Surgical Treatment of Stress Urinary Incontinence

Urinary IncontinencePelvic Floor Disorders

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.

Recruiting2 enrollment criteria

Long-term Outcomes of Autologous Transobturator Rectus Fascia Sling for Treatment of Female Stress...

Stress Urinary Incontinence

Autologous transobturator sling placement is associated with excellent short-term results and can be performed on an outpatient basis in most cases, so long-term outcomes needs to be verified.

Recruiting15 enrollment criteria

Use of a Dual-agent Local Analgesic (Bupivacaine-meloxicam) for Abdominal Incisions in Patients...

Stress Urinary IncontinenceSurgical Incision1 more

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.

Recruiting11 enrollment criteria

ProACT Post-Approval Study

Stress Urinary Incontinence

The ProACT Post Approval Study is a 5-year prospective, open-label, multi-center study designed to evaluate the long-term incidence of urethral stricture and device erosion after ProACT implantation. In addition, the study will evaluate whether treatment with ProACT affects clinical outcomes after subsequent SUI therapies.

Recruiting26 enrollment criteria

Radiofrequency in the Female Stress Urinary Incontinence

Urinary Stress Incontinence

Urinary stress incontinence ( SUI ) is defined as an involuntary loss of urinary Complaint no effort According to the Consensus of the International Continence Society (Society Continence International - ICS) . SUI Prevalence of adult female Population and 25 % to 30 %.However, despite the high prevalence, many women who have symptoms of SUI or not seek treatment remain without resolution of symptoms.Then there is the possibility of using non-invasive radiofrequency and non-ablation in external urethral meatus in order to stimulate collagen production, as one of the pathophysiological mechanisms of stress urinary incontinence is the collagen deficit in the urethral wall. It is a randomized clinical trial and the group experimental will utilize radiofrequency and kinesiotheraphy ( clinical and in home) and the group control utilize turn off- radiofrequency and kinesiotherapy (clinical and in home). The protocol f the kinesiotherapy is the same both the group, and the protocol radiofrequency the group experimental will 5 sessions (one per week) with temperature 38ºC during 2 minutes. The group control will 5 sessions (one per week) but the radiofrequency will off but glycerin is heated, for masking for the patient, during 2 min. The result of the treatment is assessed by pad test 1 hour and have others outcomes ( quality of life- Sf-26 ans King Health- and sexual function- FSFI questionaire)

Recruiting6 enrollment criteria

Laparoscopic Burch Colposuspension Versus Modified Burch Colposuspension

Stress Urinary IncontinenceBurch Colposuspention

This study aims to compare the success rate and complications following laparoscopic standard Burch colposuspension and laparoscopic modified Burch colposuspension (Transobturator tape like)

Recruiting12 enrollment criteria

Local Anesthesia Before Bulkamid Injection

Stress Urinary IncontinenceIntrinsic Sphincter Deficiency

While recommended pre-anesthesia for polyacylamide hydrogel (PAHG, Bulkamid) injections for stress urinary incontinence and intrinsic sphincter deficiency can include intraurethral anesthetic gel with or without periurethral block, there is no existing literature to guide choice of anesthesia. This is a single-blinded randomized control trial to evaluate post-procedure pain with choice of anesthesia before PAHG injection.

Recruiting9 enrollment criteria
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