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Genital Prolapse clinical trials

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NCT ID: NCT06338852 Completed - Genital Prolapse Clinical Trials

Awareness of Gynaecologists About Role of Physical Therapy in Genital Prolapse

Start date: March 3, 2023
Phase:
Study type: Observational

The aim of this study will be to detect if there is awareness of gynecologists about the role of physical therapy in genital prolapse. Physical therapy plays an important role in assessment, prevention and treatment of pelvic floor dysfunction and genital prolapse, it helps to stimulate and strength pelvic floor muscle. Physical therapy treatments for the pelvic floor may include bladder training, pelvic floor muscles training with or without biofeedback, vaginal cones, electro stimulation or other adjuncts to training.

NCT ID: NCT04856709 Completed - Genital Prolapse Clinical Trials

Abdominal Pectopexy Versus Abdominal Sacral Hysteropexy.

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

This study aims to compare between abdominal pectopexy and abdominal sacral hysteropexy in terms of efficacy (assessed by POP-Q system), intra and postoperative complications.

NCT ID: NCT03901586 Completed - Genital Prolapse Clinical Trials

Satisfaction and Long-term Anatomic Efficacy Study on Patients Who Underwent a Richter Intervention in the Obstetric and Gynecology Department of Foch Hospital Since 2008

RICHTER
Start date: December 1, 2018
Phase: N/A
Study type: Interventional

Satisfaction and Long-term Anatomic Efficacy will be assessed on Patients Who Underwent a Richter Intervention in the Obstetric and Gynecology Department of Foch Hospital Since 2008.

NCT ID: NCT02585544 Completed - Genital Prolapse Clinical Trials

Ambulatory Prolapse Surgery

PROLAMBU
Start date: October 15, 2015
Phase: N/A
Study type: Interventional

Day surgery is performed in the same way as in full hospital admission, allowing same-day discharge without increased risk. It provides many grounds for patient satisfaction. Progress in surgical and anesthesia techniques now allows this form of management to be developed and prioritized. Day-care surgery for prolapse has been little studied. The present study is intended to help extend its future implementation, the primary objective being to assess the feasibility of the day-care approach in prolapse surgery. The secondary objectives are to study criteria of non-eligibility for day-care prolapse surgery, reasons for patients' refusal, causes of failure, predictive factors for failure, patient satisfaction, postoperative complications, 2-year anatomic and functional results, pain, quality of life and sexuality, and postoperative onset of dyspareunia and urinary incontinence. The design is for a prospective non-randomized study conducted in 3 gynecologic surgery sites managed by the Lyon hospitals board (Hospices Civils de Lyon).

NCT ID: NCT00747370 Completed - Clinical trials for Stress Urinary Incontinence

Dynamic MRI of the Behaviour of Female Pelvic Floor

Start date: January 2002
Phase: Phase 0
Study type: Interventional

The purpose of this study was to test the suitability of dynamic magnetic resonance imaging for the pelvic floor floor, bladder neck and urethra in healthy volunteers, in stress incontinent patient and in women with genital prolapse.

NCT ID: NCT00551551 Completed - Clinical trials for Urinary Incontinence

Prenatal Pelvic Floor Prevention (3PN)

Start date: November 2007
Phase: Phase 3
Study type: Interventional

Objective: Compare pelvic floor disorders (urinary incontinence, anal incontinence, genital prolapse, perineal pain, sexual troubles) 12 month after a first delivery between a group of women with prenatal pelvic floor exercises and a control group. Hypothesis: Prenatal pelvic floor exercises reduce postpartum urinary incontinence.