Pelvic Floor Contraction in Different Positions Among Women With & Without

Status Completed

Clinical Trial Summary

Examination of pelvic floor contraction in different positions among women with and without stress urinary incontinence (SUI) will be conducted via diagnostic ultrasound. This will enable clinicians and researchers to establish an appropriate protocol for pelvic floor muscle examination and treatment.

Clinical Trial Description

The main goal of this study is to compare the ability of the pelvic floor muscles to contract in different positions among women suffering from SUI to healthy women. Secondary objectives: is to compare subjective reports of the difficulty to contract the pelvic floor muscles between the two groups, and to examine the connection between the severity of urinary leakage and the ability to contract pelvic floor muscles. The study will include 50 female participants in the ages of 18-45. Research group will include 25 participants suffering from SUI in accordance with the International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF) and 25 healthy participants (grade 0 on the ICIQ-SF questionnaire). The examination will be performed with an abdominal ultrasound device in supine, sitting, standing and squatting. The Height of the bladder base will be measured during rest period and maximal contraction. The extent and direction of bladder base movement would indicate the quality of pelvic floor performance. Next, the length of contraction time will be measured. The participant would hold the maximal contraction as long as possible in order to examine muscular endurance. Rest will be given between tests. After finishing the tests in all four postures, the participants will be questioned about the degree of difficulty contracting the pelvic floor. Significance of the study: The importance of the research is about granting the clinicians and researchers additional tools in order to help establishing a protocol for pelvic floor muscle activity examination and treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04288648
Study type	Observational [Patient Registry]
Source	University of Haifa
Contact
Status	Completed
Phase
Start date	May 17, 2020
Completion date	November 1, 2021

View Details

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT02867748` - TVT-ABBREVO Versus SERASIS for the Treatment of Female Urinary Stress Incontinence: 1 Year Outcomes of a Comparative Study With 2 Trans-obturator Sub Mid Urethral Slings	N/A
Recruiting	`NCT02617797` - Radiofrequency in the Female Stress Urinary Incontinence	N/A
Active, not recruiting	`NCT02538991` - TVT Versus Bulkamid®-Injections in Treatment of Stress Urinary Incontinence	N/A
Completed	`NCT02480231` - Mid-Urethral Sling Tensioning Trial	N/A
Terminated	`NCT02591381` - Transcorporal Versus Standard Artificial Urinary Sphincter Placement	N/A
Completed	`NCT00984958` - Bulkamid Treatment of Stress Incontinence in Women With Urinary Stress Incontinence and Not Suitable to TVT-procedure	N/A
Completed	`NCT00190567` - Biomechanical Effects of Duloxetine on Bladder and Sphincter Muscle Function in Women in Pure Genuine Stress Incontinence	Phase 2
Completed	`NCT02423486` - The Comparison of Efficacy Between Electromagnetic Stimulation Therapy and Electromagnetic Stimulation Therapy With Extracorporeal Biofeedback	N/A
Completed	`NCT01754558` - One Year Outcome Using the Ajust System for Treatment of Urinary Stress Incontinence	N/A
Recruiting	`NCT00136071` - Transvaginal Tension Free Vaginal Tape-Obturator (TVT-O) Versus Transobturator Tape-Mentor (TOT) in the Management of Urodynamic Stress Urinary Incontinence	N/A
Completed	`NCT00190619` - Efficacy and Safety of Duloxetine	Phase 3
Active, not recruiting	`NCT05182632` - Tele-rehabilitation Group Program for Urinary Incontinence in Older Women	N/A
Completed	`NCT03672461` - A Group-Based Therapeutic Yoga Intervention for Urinary Incontinence in Ambulatory Older Women	N/A
Completed	`NCT02407145` - Safety and Efficacy of PVDF (DynaMesh®-SIS Soft) Retropubic Midurethral Slings in Stress Urinary Incontinence in Women
Completed	`NCT01784172` - Efficacy and Safety Study of Electroacupuncture for Simple Female Stress Urinary incontinence-a Multicenter Trial	Phase 2
Not yet recruiting	`NCT06469320` - Urinary Incontinence and Other Pelvic Floor Dysfunctions in Trail Runners
Recruiting	`NCT02935803` - A Study on the Anti-incontinent Effectiveness of the mTVM Method in POPQ Stage II-III Patients	N/A
Active, not recruiting	`NCT02039830` - Group Versus Individual Physiotherapy for Urinary Incontinence in Aging Women	N/A
Recruiting	`NCT04817839` - Optimal Duration of Post-Operative Activity Restriction After Midurethral Sling Procedures	N/A
Completed	`NCT03439527` - Multisystem Cell Therapy for Improvement of Urinary Continence	Phase 1

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Pelvic Floor Contraction in Different Positions Among Women With and Without Stress Urinary Incontinence

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms