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Pelvic Organ Prolapse clinical trials

View clinical trials related to Pelvic Organ Prolapse.

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NCT ID: NCT04996563 Completed - Clinical trials for Pelvic Organ Prolapse

Patient Educational Video for Pelvic Organ Prolapse

Start date: August 2, 2021
Phase: N/A
Study type: Interventional

This is a single-blinded, randomized controlled trial investigating if a patient educational video on pelvic organ prolapse improves patient understanding of this pelvic floor disorder and satisfaction in their healthcare decision making for its management.

NCT ID: NCT04980196 Completed - Urogenital Prolapse Clinical Trials

Is Preoperative Urodynamics Essential for Women With Pelvic Organ Prolapse

urodynaemics
Start date: September 20, 2020
Phase:
Study type: Observational

urodynamic investigation when added in the diagnostic work-up of women with lower urinary tract dysfunction with POP is debatable. This study was planned to determine the usefulness of preoperative urodynamic study in improving urological outcome following surgery in women with pelvic organ prolapse and urinary tract dysfunction.

NCT ID: NCT04954443 Completed - Clinical trials for Pelvic Organ Prolapse

Urinary Retention After Removing Urinary Catheter at 24 Hour Versus 48 Hour in Patients With Vaginal Surgery

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

Comparison incident of urinary retention in patients with vaginal surgery of pelvic organ prolapse, who removed urinary catheter at 24 hours versus 48 hours after surgery

NCT ID: NCT04897061 Completed - Clinical trials for Pelvic Organ Prolapse

Caregiver Support and Post-operative Convalescence

Start date: May 24, 2021
Phase:
Study type: Observational

This is a prospective cohort study designed to investigate the impact of home caregiver support on post-operative convalescence in patients undergoing same day discharge after major urogynecologic surgery. Questionnaires assessing post-operative convalescence will be distributed at several time points after surgery. The main hypothesis is that increased caregiver support in the post-operative period will improve post-operative convalescence of patients undergoing major urogynecologic surgery.

NCT ID: NCT04852991 Completed - Clinical trials for Pelvic Organ Prolapse

Modified Purandare's Cervicopexy Versus Abdominal Sacral Hysteropexy

Start date: April 15, 2020
Phase: N/A
Study type: Interventional

This study aims to compare safety, efficacy and complications of modified Purandare's cervicopexy with abdominal sacral hysteropexy as conservative surgery in the treatment of genital prolapse in reproductive age group patients at Ain Shams Maternity hospital.

NCT ID: NCT04829721 Completed - Clinical trials for Urinary Incontinence

Pelvic Floor Disorder Assessment of Knowledge and Symptoms: an Educational Model in Spanish-Speaking Women

PAKS
Start date: May 1, 2021
Phase: N/A
Study type: Interventional

Pelvic floor health workshops have previously been shown to be effective in improving postpartum knowledge, performance of pelvic floor muscle exercises, and bowel-specific quality of life. Group learning through a class focused on behavioral modification and pelvic floor muscle exercises for women with urinary incontinence, has been shown to be an effective means to educate women about urinary incontinence management. The PAKS study hopes to demonstrate whether Spanish-speaking women that undergo an informative workshop on pelvic floor disorders via video in Spanish are more likely to raise their level of knowledge surrounding pelvic floor disorders and improve the pelvic floor symptoms.

NCT ID: NCT04824820 Completed - Clinical trials for Urinary Incontinence

Improving Female Sexual Wellness

Start date: April 10, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of commercially available genital vibrator use on sexual health, female pelvic floor disorders, and overall quality of life among a diverse population of women.

NCT ID: NCT04804826 Completed - Clinical trials for Pelvic Organ Prolapse

Same Day Discharge Following Pelvic Reconstructive Surgery

Start date: June 14, 2021
Phase:
Study type: Observational

This is a prospective cross-sectional study in which patients undergoing major pelvic reconstructive surgery with total vaginal hysterectomy will be recruited and enrolled. At approximately 2 weeks and 12 weeks postoperatively, enrolled patients will be asked to complete a survey detailing their experience with SDD, surgical recovery, and advice for prospective patients.

NCT ID: NCT04793126 Completed - Clinical trials for Pelvic Organ Prolapse

Clinical and Urodynamic Evaluation of Surgical Repair of Pelvic Organ Prolapse Associated With Lower Urinary Tract Symptoms

Start date: December 1, 2014
Phase: Phase 2
Study type: Interventional

To assess the urinary symptoms and urodynamic findings concomitant with Pelvic organ prolapse before and after surgical treatment and to define the role of urodynamic study in treatment decision making.

NCT ID: NCT04733885 Completed - Clinical trials for Pelvic Organ Prolapse

Electrical Stimulation in Women With Pelvic Organ Prolapse

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to search the effects of electrical stimulation on clinical symptoms such as pelvic floor muscle strength, stage of POP, symptoms of pelvic floor, quality of life and sexual function in women with pelvic organ prolapse (POP)