Clinical Trials Logo

Clinical Trial Summary

This study aimed to evaluate primarily the functional outcomes and secondly the morphological outcomes for women who had received standard managements for cystocele at mediate-term follow-up.


Clinical Trial Description

Pelvic organ prolapsed (POP) is an important health issue for women all over the world, with cystocele being the commonest type of POP. The side effects related to cystocele include voiding dysfunction, urinary retention, urinary tract infection, hydroureter, or hydronephrosis. The management for cystocele can be classified as non-surgical and surgical methods. Non-surgical methods comprise pelvic floor muscle exercise and vaginal pessaries, while surgical methods can be divided as conventional operations and operations applying mesh augmentation. Conventional surgeries for cystocele such as anterior colporrhapy have high surgical failure rates and complications including vaginal shortening or vaginal stenosis. Operations applying mesh augmentation are becoming the mainstream in the surgeries for cystocle. The Perigee System (American Medical Systems, Minnetonka, MN, USA), which has been approved by American FDA and Taiwan DOH in treating female cystocele, have promising short-term surgical outcomes. However, long-term reports incorporating both functional and morphological outcomes are lacking in the literatures. This study aimed to evaluate primarily the functional outcomes and secondly the morphological outcomes for women who had received standard managements for cystocele at mediate-term follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04481906
Study type Observational
Source Cathay General Hospital
Contact
Status Completed
Phase
Start date October 25, 2011
Completion date October 5, 2014

See also
  Status Clinical Trial Phase
Completed NCT01637441 - Prosthetic Pelvic Organ Prolapse Repair N/A
Recruiting NCT04009694 - Does a High BMI Affect Supervised Pelvic Floor Muscle Training for Improving Symptoms in Women With Various Stages of Pelvic Organ Prolapse? N/A
Completed NCT02888093 - A Randomized Controlled Trial of Permanent vs Absorbable Suture for Uterosacral Ligament Suspension N/A
Completed NCT02272361 - Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair. N/A
Completed NCT02255994 - UGYTEX® Mesh Versus Subvesical Plication in the Surgical Treatment of Bladder Prolapse N/A
Withdrawn NCT00942474 - Nerve Access Tool Study N/A
Completed NCT04417413 - Safety and Efficacy of Non-ablative Er:YAG Laser Therapy for the Treatment of Pelvic Organ Prolapse and Coexisting Stress Urinary Incontinence: A Retrospective Case Series.
Active, not recruiting NCT03714607 - Laser Therapy in Managing Vaginal Prolapse N/A
Completed NCT04184128 - Detrusor Underactivity and Bladder Outlet Obstruction in Women With Cystocele
Active, not recruiting NCT01097200 - Sacrocolpopexy Versus Vaginal Mesh Procedure for Pelvic Prolapse N/A
Recruiting NCT00162604 - Prophylactic Antibiotic Treatment During Vaginal Repair N/A
Completed NCT02400034 - Comparing Voiding Trials After Midurethral Sling for Stress Incontinence N/A
Completed NCT01559558 - Changes of Pad Weight Results and Urethral Pressure Profiles After Reduction of Cystocele by Vaginal Gauze Packing N/A
Not yet recruiting NCT03056586 - The Effect of Pessary Post Vaginal Prolapse Repair, for One Month, to Reduce the Recurrence Rate of Prolapse N/A
Active, not recruiting NCT02272322 - Transvaginal Treatment of Symptomatic Cystocele Grade II-III N/A
Completed NCT00557882 - Efficacy Study of Vaginal Mesh for Anterior Prolapse Phase 4
Completed NCT06410469 - A Novel Suturing Technique of Cystocele Treatment
Completed NCT04175782 - Enhanced Recovery Protocol in Urogynecologic Surgery N/A
Recruiting NCT05449054 - Continuous Stitches Versus Simple Interrupted Stitches for Anterior Colporrhaphy N/A
Recruiting NCT05688059 - Absorbable Suture vs Permanent Suture in Sacrospinous Ligament Suspension N/A