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Urinary Incontinence, Stress clinical trials

View clinical trials related to Urinary Incontinence, Stress.

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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: NCT03082118 Completed - Clinical trials for Stress Urinary Incontinence

Vesair Continued Access Trial

VESICAL
Start date: March 9, 2017
Phase: N/A
Study type: Interventional

Single arm study of the Vesair Balloon in postmenopausal women.

NCT ID: NCT03073824 Completed - Sexual Dysfunction Clinical Trials

A Long-term Evaluation of a Novel Intravaginal Device

Start date: March 6, 2017
Phase: N/A
Study type: Interventional

An open-label long-term evaluation of a novel intravaginal device in female patients experiencing sexual and bladder function issues.

NCT ID: NCT03066180 Completed - Clinical trials for Stress Urinary Incontinence

Study of Non-Ablative Radiofrequency Treatment for Stress Urinary Incontinence

Start date: May 29, 2017
Phase: N/A
Study type: Interventional

This is a prospective, pilot clinical study involving two study groups. This study is designed to demonstrate that the study treatment meets primary efficacy and safety endpoints. The treatment involves radiofrequency treatment to address symptoms of stress urinary incontinence. After receiving the study treatment, subjects will be followed out to 12 months post-treatment. At the Screening Visit, and at each designated follow-up timepoint, subjects will be asked to complete a variety of questionnaires, provide a patient diary, and undergo an objective assessment for urine loss.

NCT ID: NCT03058042 Completed - Clinical trials for Urinary Incontinence, Stress

Outpatient and Home Pelvic Floor Training for Stress Urinary Incontinence

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

The objective of this study is to compare the effect of outpatient pelvic floor muscle training versus home pelvic floor muscle training in the treatment of stress urinary incontinence. The hypothesis of this study is that home pelvic floor muscle training is as effective as outpatient pelvic floor muscle training for the treatment of stress urinary incontinence.

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.

NCT ID: NCT03048682 Recruiting - Surgery Clinical Trials

Timing of Repeat Voiding Trials After Outpatient Pelvic Floor Surgery

Start date: January 5, 2017
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial designed to assess the rate of failure of voiding trials in the early and late post-operative period within patients who underwent outpatient pelvic floor surgery that failed initial same day voiding trials.

NCT ID: NCT03037008 Completed - Clinical trials for Urinary Incontinence, Stress

Perineal Ultrasound in Men Before and After Radical Prostatectomy

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

Prospective study to evaluate a new technique. Comparison of perineal sonography in men before and after radical prostatectomy and in incontinent men after radical prostatectomy before and after operative treatment with male sling and comparison with pre- and postoperative functional MRI Inclusion / Exclusion criteria: Inclusion: male, elder than 18years, planned RALP or history of RALP and PPSUI (Post Prostatectomy Stress Urinary Incontinence). Exclusion: Patients with history of urinary incontinence before radical prostatectomy. Patients with history of radiotherapy in the pelvis. Other diseases involving pelvic floor.

NCT ID: NCT03010800 Completed - Clinical trials for Stress Incontinence, Female

A Feasibility Device Study to Prevent Female Urinary Stress Incontinence

Start date: January 4, 2017
Phase: N/A
Study type: Interventional

This study will test the acute efficacy of an investigational device (Yoni.Fit) in a clinical trial of women with incontinence in a standardized set of challenges performed with and without the device in place.

NCT ID: NCT03005977 Completed - Clinical trials for Pelvic Organ Prolapse

Identifying Stress Urinary Incontinence in Women With Pelvic Organ Prolapse

Start date: February 15, 2017
Phase: N/A
Study type: Interventional

What test is most sensitive in identifying stress urinary incontinence in women with pelvic organ prolapse; urodynamics, cough stress test, or pyridium pad test? The hypothesis states that there is a difference between the sensitivity of UDS, pyridium pad test and cough stress tests, with UDS being the most sensitive and the gold standard in identifying SUI in patients with pelvic organ prolapse.