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Pelvic Organ Prolapse clinical trials

View clinical trials related to Pelvic Organ Prolapse.

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NCT ID: NCT01632839 Completed - Clinical trials for Urinary Incontinence

Psychometric Validation of a French Version of the PISQ-R and a New Questionnaire About Sexuality

Start date: January 18, 2013
Phase:
Study type: Observational

The primary objective of this study is the psychometric validation of two questionnaires (PISQ-R and a new questionnaire on sexuality) as compared to a non specific questionnaire on female sexual function (FSFI).

NCT ID: NCT01618994 Completed - Clinical trials for Pelvic Organ Prolapse

Validation Study for Robotic Surgery Simulator

Start date: April 2011
Phase: N/A
Study type: Observational

A study to determine whether completing a rigorous simulation protocol could provide novice robotic surgeons with actual advanced surgical skills in an operating room setting.

NCT ID: NCT01618292 Completed - Clinical trials for Irritable Bowel Syndrome

Cohort Study of Bowel Function Following Robotic-assisted Laparoscopic Sacrocolpopexy

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

Compare changes in bowel function before, 6 months and one year after Robotic-assisted laparoscopic sacral colpopexy. Compare objective anatomic outcomes before, 6 months and one year after Robotic-assisted laparoscopic sacral colpopexy.

NCT ID: NCT01614587 Completed - Clinical trials for Pelvic Organ Prolapse

Do Patients With Early Post Operative Recurrence of Pelvic Organ Prolapse Have a Genetic Predisposition?

Start date: March 2012
Phase: N/A
Study type: Observational

The objective is to explore the genetic predisposition to early pelvic organ prolapse after adequate surgical repair by exploring the association between pelvic organ prolapse recurrences and certain polymorphisms.

NCT ID: NCT01612637 Completed - Clinical trials for Pelvic Organ Prolapse

Can Pelvic Floor Muscle Training Reduce my Prolapse

Start date: August 2012
Phase: N/A
Study type: Interventional

Purpose The aim of this study is to examine if a structured pelvic floor muscle training combined with lifestyle advice with can improve pelvic organ prolapse (POP) symptoms more than structured lifestyle advice programme alone. Background Pelvic organ prolapse (POP) is a common condition among adult women and almost one in ten women experience symptoms caused by POP. The key symptom of POP is seeing or feeling a bulge in the vaginal opening but POP often gives other symptoms, such as pain, difficulty emptying the bladder or the bowel, incontinence and sexual problems such as dyspareunia. A majority of women with POP will be offered reconstructive surgery but the risk of reoperations is substantial and surgery may cause new symptoms. In one out of four women surgery does not relieve symptoms and the women have been exposed to unnecessary risk of complications. It is therefore important to evaluate the effect of conservative treatments for POP. New studies have shown that pelvic floor muscle training offered in combination with lifestyle advice has a significant on POP symptoms and objective measures of POP compared to a lifestyle advice leaflet alone. No studies have compared the effect of a combined pelvic floor muscle training and lifestyle advice programme with a structured programme of lifestyle advice and hypothetically the structured lifestyle advice programme could have a substantial effect on its own. Our hypothesis is that the pelvic floor muscle training is a vital component of a conservative treatment for POP. Methods In this single-blind randomised controlled study women with POP will randomised to either a programme of structured pelvic floor muscle training combined with lifestyle advice or a structured lifestyle advice programme alone. Both groups will receive the same lifestyle advices through six (separate) lectures within 12 weeks. The training group will be examined and individually instructed in pelvic floor muscle training before the intervention starts and they will, in continuation with their lifestyle lectures, perform pelvic floor muscle training as group training

NCT ID: NCT01611285 Completed - Clinical trials for Pelvic Organ Prolapse

Uphold Versus Robotic Surgery for Pelvic Prolapse Repair: A Decision Analytic Approach

Start date: November 2010
Phase: N/A
Study type: Observational

Within the general objective of investigating optimal medical techniques for pelvic prolapse repair, this study proposes to: (1) test the hypothesis that the UPHOLD procedure is more cost effective than robotic surgery for pelvic prolapse repair (2)using formal decision analysis as the comparative strategy

NCT ID: NCT01598467 Recruiting - Clinical trials for Pelvic Organ Prolapse

Prospective Assessment of Robotic Sacrocolpopexy: a European Multicentric Cohort (PARSEC)

PARSEC
Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to prospectively assess the outcomes of robotic sacrocolpopexy for repair of pelvic organ prolapse in high volume european centers.

NCT ID: NCT01597544 Active, not recruiting - Clinical trials for Voiding Dysfunction After Pelvic Organ Prolapse Surgery

Post-operative Voiding Dysfunction: the Preferred Method for Catheterization

Start date: July 2012
Phase: N/A
Study type: Interventional

This study is divided into two parts. The first part is a prospective observational study of patients undergoing pelvic organ prolapse (POP) surgery. The goal is to determine patient preference between 3 different methods of bladder drainage in case of post-operative voiding dysfunction (POVD): transurethral indwelling catheterization (TIC), clean intermittent self-catheterization (CISC), and suprapubic tube (SPT). The second part of the study will be for those that choose CISC as their preferred method, whereby these patients will be randomized to receive CISC instruction either pre- or post-operatively to determine whether there is a difference in overall patient satisfaction based on timing of teaching. The investigators hypothesize that patients that receive informed consent pre-operatively will favour the use of SPT over TIC and CISC to manage potential POVD. Among those patients who opted for CISC in management of their post-operative voiding dysfunction, patients that are taught how to perform CISC pre-operatively in the clinic will have a higher level of satisfaction compared to those that are taught post-operatively in the hospital.

NCT ID: NCT01590576 Completed - Clinical trials for Pelvic Organ Prolapse

Population-based Estimates of Medical Comorbidities in Women With Lower Urinary Tract Symptoms or Pelvic Organ Prolapse

Start date: November 2014
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the comorbidities of lower urinary tract symptoms or pelvic organ prolapse in a nationwide population-based data in Taiwan during the study period of 2001-2010, a total of 10 years.

NCT ID: NCT01559168 Completed - Clinical trials for Pelvic Organ Prolapse

Uphold Mesh for the Surgical Treatment of Uterine-predominant Prolapse

Start date: October 2012
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of the UpholdTM LITE mesh over a 12 month follow up period, using a composite outcome including a good anatomical correction for both anterior and apical compartments (stage 0 or 1), no prolapse (bulge) symptoms (answer "no" at question 3 of the PFDI-20) and no reintervention for recurrent prolapse of the anterior or apical compartment.