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Pelvic Floor Disorders clinical trials

View clinical trials related to Pelvic Floor Disorders.

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NCT ID: NCT02259712 Completed - Clinical trials for Urinary Incontinence

Effectiveness of Hypopressive Exercises Versus Pelvic-perineal Physiotherapy

HEPFD
Start date: October 2013
Phase: N/A
Study type: Interventional

Introduction: Hypopressive Exercises are included within a method of physiotherapy which was created with the purpose of strengthening the deep muscles of the abdomen without damaging ligamentous and muscular structures of the perineum, also strengthening the muscles of pelvic floor reflexively. Although this technique has been included as treatment and a prevention method of pelvic floor dysfunction, there are few studies supporting its benefits. The investigators hypothesis is that the combination of both physiotherapy treatments will provided the best results for women who suffer pelvic floor dysfunctions. Objective: To determine whether Hypopressive Exercises are an option to include in the physiotherapy treatment of women suffer at least one pelvic floor dysfunction and whether the results reported are comparable to those provided by pelvic-perineal physiotherapy. Subjects and methods: A randomized clinical trial, the examiner being blinded unaware of the intervention group to which subjects were assigned. Participants will be randomly assigned to three groups: 1. An experimental group, where the participants will be treated by Hypopressive exercises and hygienic and behavioral measures; 2. Another experimental group where pelvic-perineal physiotherapy will join with Hypopressive exercises and hygienic and behavioral advises; 3. And a third group where will be done pelvic-perineal physiotherapy and hygienic and behavioral measures. Pre- intervention, immediate post-intervention, 3, 6 and 12 months assessments will be made. The selection criteria will be: adult women who present signs and symptoms that indicate a pelvic floor dysfunction or have a medical diagnosis to confirm it. All participants must understand and sign freely Informed Consent. Sample size: Accepting an alpha risk of 0.05 and a beta risk of 0.2 in a bilateral contrast, 26 subjects were required in each group to detect a difference equal to or greater than 3 microvolts (Total of 78 subjects). It assumes a standard deviation of 4.8 microvolts and the rate of loss to follow up esteem 20% (Magalhães-Resende et al. 2012). Data Analysis: A descriptive analysis of all variables was performed. It establish for all cases a confidence level of 95% (p <0.05). The effectiveness was assessed by comparing the experienced change of the three goups in outcome variables between physicaltherapy examinations.

NCT ID: NCT02176330 Completed - Clinical trials for Pelvic Floor Disorders

Does Using a 'Virtual Clinic' in Urogynaecology Improve Patient Experience and Reduce Cost?

Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the impact of using a virtual clinic which combines a web-based interactive questionnaire (ePAQ-PF) used in advance of clinic appointments in combination with a telephone consultation has on patient experience and cost compared to standard care.

NCT ID: NCT01938092 Completed - Pelvic Pain Clinical Trials

Vaginal Diazepam for the Treatment of Female Pelvic Pain

Start date: September 2013
Phase: Phase 2
Study type: Interventional

To determine the efficacy of intravaginal diazepam for the treatment of pelvic pain associated with pelvic floor hypertonic disorder.

NCT ID: NCT01612156 Completed - Clinical trials for Pelvic Floor Disorders

Lubricant Versus Lidocaine Gel for Pain Control During Urodynamics

Start date: December 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine a difference in patient reported pain levels before, during, and after multichannel urodynamics in patients treated with 2% lidocaine gel or water based lubricant. We hypothesize that lidocaine gel will decrease pain levels when compared to lubricant gel.

NCT ID: NCT01370122 Completed - Ovarian Cancer Clinical Trials

Pelvic Floor Disorders in Survivors of Gynecologic Malignancies

Start date: May 2011
Phase:
Study type: Observational

Pelvic Floor dysfunction affects the quality of life of women. However, the prevalence and risk factors for pelvic floor disorders (PFD) in survivors of gynecologic malignancies are not known. The investigators plan to perform an observational study including survivors of gynecologic malignancies. Questionnaires for diagnosis of pelvic floor disorders will be mailed to survivors to generate prevalence rates and risk factors for PFD in women with a history of a gynecologic cancer diagnosis.

NCT ID: NCT01288703 Completed - Clinical trials for Urinary Incontinence

Computerized-Adaptive Testing: Feasibility In Women With Pelvic Floor Disorders (CAT)

CAT
Start date: August 2010
Phase: N/A
Study type: Observational

The objective of this pilot-study is to evaluate the feasibility and acceptability of PROMIS computerized-adaptive testing in women with urinary incontinence.

NCT ID: NCT00952406 Completed - Clinical trials for Pelvic Organ Prolapse

A Multi Center Study to Validate a Condition-specific Measure of Sexual Health in Women With Pelvic Floor Disorders

Start date: August 2009
Phase: N/A
Study type: Observational

Study Aims: 1. To validate a new measure of sexual function and activity in women with PFDs; 2. To establish the responsiveness to change of the new measure. The investigators hypothesis is that the investigators can create a new questionnaire that accurately measures sexual health in women with pelvic floor disorders that improves on the already published questionnaires.

NCT ID: NCT00884871 Completed - Clinical trials for Pelvic Floor Disorders

Study of Surgically-Induced Weight Loss on Pelvic Floor Disorders

Start date: September 2007
Phase: N/A
Study type: Observational

The specific aim of this study is to evaluate the effect of surgically-induced weight reduction, as achieved by laparoscopic gastric banding or sleeve gastrectomy, on pelvic floor disorders such as stress urinary incontinence, overactive bladder, anal incontinence, and pelvic organ prolapse in severely, morbidly and super-obese women using a prospective, observational study design.

NCT ID: NCT00880880 Completed - Clinical trials for Urinary Incontinence

Improving Women's Health by Using an Electronic Pelvic Floor Questionnaire

Start date: August 2007
Phase: N/A
Study type: Interventional

The overall goal of this study is to test whether an electronic pelvic floor questionnaire (e-PAQ-PF) will increase discussion rates of incontinence in a primary care setting.