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Pelvic Organ Prolapse clinical trials

View clinical trials related to Pelvic Organ Prolapse.

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NCT ID: NCT01917968 Completed - Clinical trials for Pelvic Organ Prolapse

Uphold LITE Post-Market Surveillance Study

Uphold LITE
Start date: October 10, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare transvaginal mesh repair to traditional native tissue repair in women surgically treated for anterior and/or apical pelvic organ prolapse.

NCT ID: NCT01886794 Terminated - Clinical trials for Pelvic Floor Disorders

Hormonal Status on Blood Flow and Tissue in Pelvic Organ Prolapse

Start date: June 6, 2013
Phase: Phase 4
Study type: Interventional

Our primary aim in the current study is to determine important tissue differences, including muscle and connective tissue changes, between postmenopausal women and reproductive age women with pelvic floor dysfunction to help develop targeted and noninvasive treatments.

NCT ID: NCT01864408 Completed - Clinical trials for Pelvic Organ Prolapse

Interactive Web-Based Tool for Pelvic Organ Prolapse: Impact on Patient Understanding and Provider Counseling

iPad
Start date: May 2012
Phase: N/A
Study type: Interventional

The primary aim is to assess whether an interactive patient/provider counseling process using a web-based tool (iPadTM) will improve patient satisfaction regarding understanding of her bulge symptoms. The secondary aims are to assess whether an interactive patient/provider counseling process using web-based tool (iPadTM) will: 1. Decrease patient anxiety with counseling 2. Improve patient satisfaction with counseling 3. Improve provider knowledge, anxiety, and satisfaction with counseling 4. Be easy to use in clinic 5. Be actually used in clinic

NCT ID: NCT01852422 Completed - Clinical trials for Pelvic Organ Prolapse

Location and Anatomic Characterization of the Sacrospinous Ligaments in Women With Pelvic Organ Prolapse

Start date: June 2013
Phase:
Study type: Observational

Pelvic organ prolapse is a common disorder that results in significant patient morbidity. Approximately 1 in 9 women undergo surgery for the correction of pelvic organ prolapse (POP) and associated bladder and bowel dysfunction. Despite its common occurrence, the cause of POP remains largely unknown. Prolapse is thought to be caused by direct injury to the levator ani (LA) muscle, denervation of the pelvic floor musculature, or fascial damage incurred during childbirth trauma. The sacrospinous ligaments are commonly employed surgical structures employed to repair vaginal prolapse. Despite the frequent use of these structures in prolapse surgery, there is a paucity of information regarding the identification of these structures outside of surgical dissection. Furthermore, there is no published data describing the relative distances between the apex of the vagina and these ligaments in women with prolapse. Recent developments in imaging have enabled the identification of the distal subdivisions of the levator ani, classifying as: pubovaginalis, puboanalis, and the puboperinealis as the subdivisions of the pubovisceralis. The visualization of these structures is possible using a 3D ultrasound technique (BK medical, Wilmington, MA), that has been validated in cadavers and in live humans, with excellent interrater reliability. The investigators propose to use this technology to explore the anatomy of the sacrospinous ligaments.

NCT ID: NCT01842464 Completed - Clinical trials for Pelvic Organ Prolapse

Sacro-Spinous Ligaments Anterior Apical Anchoring

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

Anterior-apical compartment mesh implants for pelvic floor reconstruction are anchored here to the Sacro-Spinous ligaments and evaluated being a feasible and effective method.

NCT ID: NCT01840176 Completed - Clinical trials for Vaginal Vault Prolapse

Prophylactic Modified McCall Culdoplasty During Total Laparoscopic Hysterectomy

Start date: May 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the feasibility of performing prophylactic McCall culdoplasty at the time of total laparoscopic hysterectomy. The investigators will also be measuring pelvic support (using POP-Q) and sexual function before and at different time points (up to 12 months) postoperatively. The investigators hypothesize that women undergoing the McCall culdoplasty will not have different immediate surgical outcomes (operative time, etc) and may have better pelvic support and sexual function in the future.

NCT ID: NCT01827774 Completed - Clinical trials for Pelvic Organ Prolapse

Soft Tissue Graft for Repair of Pelvic Organ Prolapse

POP
Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this Study is to collect information about the performance of the Surgisis® Soft Tissue Graft ("Study Product") for the repair of pelvic organ prolapse in women.

NCT ID: NCT01805310 Completed - Clinical trials for Pelvic Organ Prolapse

Pre-operative Bowel Preparation Prior to Minimally Invasive Sacral Colpopexy

Start date: February 2013
Phase: Phase 4
Study type: Interventional

Prior to surgery, gynecologists and urogynecologists have routinely prescribed preoperative mechanical bowel preparations in attempts to decrease the risk of infection, while also providing easier bowel manipulation and better visualization during surgery. However, many of these proposed benefits have never been proven, and usage of bowel preparations amongst surgeons remains highly variable. In both the general surgery and gynecology literature, researchers have begun to question the need for the vigorous preparations. Aside from surgical visualization, urogynecologists have additional concerns about how bowel preparations may impact postoperative bowel function given up to half of women with pelvic floor disorders have baseline constipation and straining is known to impact surgical recovery. Many studies have addressed various postoperative fiber and laxative preparations in attempts to improve postoperative bowel-related symptomatology, but none have specifically looked at preoperative bowel preparations. This study aims to determine if mechanical bowel preparation prior to minimally invasive sacral colpopexy affects patients' postoperative recovery, specifically related to bowel symptomatology; operative or post-operative complications; surgeons' perceptions of surgical difficulty directly attributed to the bowel; and post-operative return of normal bowel function.

NCT ID: NCT01778985 Completed - Menopause Clinical Trials

Effect of Preoperative Estrogen Treatment on Connective Tissues of the Pelvic Floor

PET
Start date: December 2012
Phase: Phase 4
Study type: Interventional

This is a study to determine how vaginal estrogen cream given for several weeks before pelvic reconstructive therapy will effect elastic fiber assembly in the muscularis layer of the vaginal wall. Postmenopausal women with at least Stage 2 pelvic organ prolapse will receive either estrogen vaginal cream or placebo cream 6-8 weeks prior to reconstructive surgery. At time of surgery, full thickness biopsies will be obtained from a standardized location at the top of vagina. The investigators will measure the thickness of the vaginal muscularis, elastic fiber number and morphology, and analyze if elastic fiber synthesis or degradation is affected by estrogen therapy. The results will provide important data to support a larger clinical trial to determine if preoperative and maintenance estrogen therapy alter long-term success rates of pelvic reconstructive surgery for pelvic organ prolapse.

NCT ID: NCT01776580 Recruiting - Clinical trials for Pelvic Organ Prolapse

The Association of Pelvic Organ Prolapse Severity and Urinary Symptoms and Sexual Function

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

Women with pelvic organ prolapse often accompany with urinary symptoms or sexual dysfunction, and analyzing the association will be helpful to identify the indication of proper management. Therefore, the aim of this study is to identify the above associations by perineal sonography.