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Prolapse clinical trials

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NCT ID: NCT03065075 Completed - Clinical trials for Urinary Retention Postoperative

Effect of Phenazopyridine on Prolapse Surgery Voiding Trials

EPOV
Start date: February 1, 2017
Phase: Phase 3
Study type: Interventional

To determine if phenazopyridine reduces the rate of postoperative urinary retention after pelvic organ prolapse surgery.

NCT ID: NCT03064750 Completed - Clinical trials for Pelvic Organ Prolapse

Pelvic Floor Exercise Before Surgery in Women With Pelvic Organ Prolapse

CONTRAPOP
Start date: January 1, 2017
Phase: N/A
Study type: Interventional

The lifetime risk for a woman to undergo surgery for either vaginal prolapse or urinary incontinence is high. There are many different surgical techniques for treatment of prolapse, but there is a lack of knowledge about factors that contribute to objective result and patient satisfaction after surgery. The aim of the study is to investigate factors that could be related to patient satisfaction and objective result such as pelvic floor muscle contractility/strength and muscle injury, objective measures of prolapse and women's symptoms. This study will investigate whether systematic pelvic floor exercise and life style advise before surgery can improve outcomes after surgery for either vaginal prolapse. Another aim is to determine an ultrasound scale for measure of pelvic floor muscle contraction.

NCT ID: NCT03052816 Completed - Pain, Postoperative Clinical Trials

Ice T Postoperative Multimodal Pain Regimen in FPMRS Surgery

ICET
Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this randomized controlled trial is to determine whether, "ICE-T," a novel multimodal postoperative pain regimen composed of around the clock ice packs, toradol, and tylenol, has improved pain control intake compared to the standard postoperative pain regimen in patients undergoing vaginal pelvic floor reconstructive surgery.

NCT ID: NCT03040011 Completed - Surgery Clinical Trials

Preoperative Levator Ani Muscle Injection and Pudendal Nerve Block for Pain Control After Vaginal Reconstructive Surgery

Start date: June 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

To test the hypothesis that preoperative injections along the levator ani muscles and pudendal nerve with bupivacaine and dexamethasone improve pain control after vaginal apical reconstructive surgery. A three-arm, double-blinded, randomized controlled trial of a total of 75 women will be performed. The study population will be adult women (>18 years of age) with uterovaginal or vaginal vault prolapse who have been scheduled for native tissue vaginal reconstructive surgery which includes an apical support procedure. Participants will be enrolled prior to surgery. The procedure will involved four injection sites: the bilateral levator ani muscles via a transobturator approach and bilateral pudendal nerves via a transvaginal approach. Random assignment will occur to one of three study arms: combined arm (20 milliliters bupivacaine/dexamethasone solution divided between the 4 injection sites), bupivacaine arm (20 milliliters bupivacaine divided between the 4 injection sites), or placebo arm (20 milliliters saline divided between the 4 injection sites).

NCT ID: NCT03034499 Completed - Clinical trials for Pelvic Organ Prolapse

Single Versus Multi-port Robotic Assisted Sacrocolpopexy for Repair of Vaginal Apex Prolapse

Start date: March 20, 2017
Phase: N/A
Study type: Interventional

A prospective randomized controlled study intended to compare the efficacy of 2 methods of robotic assisted sacrocolpopexy for the repair of vaginal apex prolapse: 1. Via single-port. 2. Via multi-port.

NCT ID: NCT03032848 Completed - Clinical trials for Pelvic Organ Prolapse

Vaginal Estrogens Comparative Trial on Pelvic Organ Prolapse Patients

Start date: November 26, 2013
Phase: Phase 4
Study type: Interventional

To evaluate the difference of three vaginal estrogens creams comparative with placebo on improvement of hormonal cytology, local and systemic climacteric complaints, as well as its endometrial security.

NCT ID: NCT03009968 Completed - Clinical trials for Urinary Incontinence

Reducing Postoperative Catheterization

Start date: March 17, 2017
Phase: N/A
Study type: Interventional

After reconstructive pelvic surgery urinary retention occurs in up to 60% of patients requiring an indwelling catheter or self-catheterization (1-5). Up to 35% of women with acute retention experience urinary tract infections in the postoperative period (6, 7). Many women consider being discharged with a Foley catheter to be a surgical complication and describe catheter use as the worst aspect of their surgery(8). At this time there is no consensus within the field of Female Pelvic Medicine and Reconstructive Surgery (FPMRS) on how to best assess voiding function postoperatively. FPMRS providers both within the United States and around the world utilize a variety of void trial methods and varying criteria to determine adequacy of post-operative voiding efficiency (5). The traditional backfill assisted void trial method involves the assessment of a postvoid residual (PVR) volume obtained either via catheterization or bladder scan (3). Recently, there have been efforts to determine ways to avoid the assessment of a PVR as it is time-consuming and potentially exposes the patient to additional catheterizations (9, 10). Many FPMRS providers utilize the backfill assisted method without assessing a PVR and instead utilize a certain voided volume threshold to determine adequate voiding. However, to date, no one has directly studied this approach or compared the traditional backfill assisted void trial to a PVR-free backfill assisted void trial. By decreasing catheterization and creating a more efficient void trial method, the investigators hope improve patients' postoperative experience and reduce catheterization and risk of urinary tract infection (UTI). This study aims to compare two void trial methodologies in order to help standardize post-operative care in the urogynecology population. This study also has potential to lead to an overall change in our field and improve the postoperative course for women across the country and abroad.

NCT ID: NCT03005977 Completed - Clinical trials for Pelvic Organ Prolapse

Identifying Stress Urinary Incontinence in Women With Pelvic Organ Prolapse

Start date: February 15, 2017
Phase: N/A
Study type: Interventional

What test is most sensitive in identifying stress urinary incontinence in women with pelvic organ prolapse; urodynamics, cough stress test, or pyridium pad test? The hypothesis states that there is a difference between the sensitivity of UDS, pyridium pad test and cough stress tests, with UDS being the most sensitive and the gold standard in identifying SUI in patients with pelvic organ prolapse.

NCT ID: NCT02971332 Completed - Rectal Prolapse Clinical Trials

Long Term Results of STARR With Contour Transtar

LTSTARR
Start date: June 2007
Phase: N/A
Study type: Observational

Obstructed defecation syndrome (ODS) is a widespread and disabling syndrome. With this study the investigators want to evaluate the long term results of Stapled Transanal Rectal Resection (STARR) performed with Contour Transtar device in the treatment of ODS. A re-evaluation of 113 patients subjected to STARR from June 2007 to January 2010 was conducted.

NCT ID: NCT02947282 Completed - Clinical trials for Pelvic Organ Prolapse, Patient Education

PREgnancy-associated Pelvic Floor Health Knowledge And REDuction of Symptoms: The PREPARED Trial

PREPARED
Start date: June 2013
Phase: N/A
Study type: Interventional

The pelvic floor is composed of muscles and connective tissue which acts to provide support for pelvic organs, and weakness or injury to the pelvic floor can result in pelvic floor dysfunction. Respect for patient autonomy is a guiding principle in medicine and is of increasing importance for patients. The PREPARED Trial hopes to demonstrate whether a single workshop on pelvic floor health during pregnancy will lead to improved knowledge of pelvic floor symptoms postpartum, increase the practice of pelvic floor muscle exercises, increase satisfaction with their delivery experience, and change participants preferences and thoughts surrounding various modes of delivery.