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Anterior Vaginal Wall Prolapse clinical trials

View clinical trials related to Anterior Vaginal Wall Prolapse.

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NCT ID: NCT06429228 Recruiting - Clinical trials for Catheter Related Complication

Comparison of 1 Versus 2 Days Post-Operative Catheterization After Anterior Colporrhaphy

Start date: April 20, 2020
Phase: N/A
Study type: Interventional

Patients who undergo anterior vaginal wall plastic surgery and place the bladder catheter during surgery are selected. The purpose of the study is to evaluate the presence of statistically significant differences in bladder catheter repositioning within 12 hours after bladder catheter removal in the group of patients in whom the bladder catheter is removed on postoperative day I or II. Secondary outcomes include evaluation of the incidence of urinary tract infections, number of hospitalization days and total hospitalization costs for patients undergoing anterior vaginal wall surgery in patients in whom the bladder catheter is removed on postoperative day I or II.

NCT ID: NCT02469584 Recruiting - Clinical trials for Anterior Vaginal Wall Prolapse

Small Stitch Study

Start date: October 2014
Phase: N/A
Study type: Interventional

A descent of the anterior vaginal wall is the most common form of female pelvic organ prolapse (POP). Although anterior colporrhaphy (AC) is accepted worldwide as a "standard procedure", its exact steps are not well standardized. We developed a small stitch anterior colporrhaphy (SSTAC) in an effort to increase the strength and durability of AC Objectives The aim of this pilot study is to demonstrate the feasibility and complication rate of the SSTAC and to assess the anatomical and functional outcomes after this method of cystocele repair.

NCT ID: NCT02209337 Completed - Clinical trials for Anterior Vaginal Wall Prolapse

Demonstrate the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse

Start date: September 2014
Phase: N/A
Study type: Interventional

A prospective, single arm, pre-market, multi-center clinical study to evaluate the safety and performance of the SRS (Lyra Medical) vaginal mesh in POP patients

NCT ID: NCT01393171 Completed - Clinical trials for Pelvic Organ Prolapse

Anterior Colporrhaphy Versus Cystocele Repair Using Polypropylene Mesh or Porcine Dermis

OARS
Start date: January 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the success rate of cystocele repair using polypropylene mesh or porcine dermis compared to that of anterior colporrhaphy in a prospective randomized fashion. The study will be performed in a randomized, prospective, single-blinded fashion.

NCT ID: NCT00420225 Completed - Clinical trials for Anterior Vaginal Wall Prolapse

Mesh Repair of Anterior Vaginal Wall Prolapse

Start date: April 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether reenforcement with polypropylen mesh compared with traditional anterior colporrhaphy for anterior vaginal wall prolapse results in fewer recurrences.