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Pelvic Organ Prolapse clinical trials

View clinical trials related to Pelvic Organ Prolapse.

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NCT ID: NCT03457883 Completed - Clinical trials for Pelvic Organ Prolapse

Risk Factors for Recurrence After Pelvic Reconstruction

Start date: January 2015
Phase: N/A
Study type: Interventional

232 women underwent transvaginal mesh repair (TVM)with /without transvaginal hysterectomy for symptomatic POP, including group A(accepted herniamesh polypropylene mesh, 117 patients);group B (underwent biological graft of cook,115 patients);follow-ups for six months and one year after the surgery and a questionnaire about the life habits associated with relapse.

NCT ID: NCT03436147 Completed - Clinical trials for Pelvic Organ Prolapse

Vaginally Assisted Laparoscopic Hysteropexy Versus Vaginal Hysterectomy

Start date: February 1, 2018
Phase:
Study type: Observational

Utero-vaginal prolapse is a common, often disabling, condition experienced by women of varying ages. The traditional surgical treatment for utero-vaginal prolapse often includes vaginal hysterectomy and anterior or posterior colporrhaphy. Growing emphasis on patient-centered medicine and patient-generated definitions of surgical success has resulted in reassessment of uterine preservation versus hysterectomy at the time of apical POP repair. Various techniques have been described for uterine preserving prolapse surgery, which may include vaginal sacrospinous hysteropexy, transvaginal mesh kits, abdominal sacrohysteropexy using mesh and laparoscopic uterine suspension using sling or mesh. A modified form of uterine-preserving prolapse surgery using a combined vaginal and laparoscopic approach was introduced and a series of 70 women was reported. To date, there have been no randomized studies comparing the outcomes of vaginal assisted laparoscopic uterine suspension (hysteropexy) with conventional vaginal hysterectomy. Women attending the gynecology clinic at a tertiary referral urogynecology unit in tertiary referral training and research hospital requesting surgical treatment for STAGE 2-4 symptomatic uterine prolapse will be offered participation in a randomized trial, over a 2-year period. Subjects participating in the study were randomly assigned to either of two groups: Group A, Vaginally Assisted Laparoscopic Hysteropexy (VALH), or Group B, Vaginal Hysterectomy and Mc Call Culdoplasty (VH + Mc Call).1 year following surgery, vaginal prolapse will be assessed again using the International Consultation on Incontinence Questionnaire for Vaginal Symptoms (ICIQ-VS) questionnaire and the Pelvic Organ Prolapse -Quantification (POP-Q) examination by another researcher then the operator.

NCT ID: NCT03427606 Active, not recruiting - Clinical trials for Pelvic Organ Prolapse

Continuous Locked Non-barbed Suture for Mesh Fixation During Laparoscopic Sacral Colpopexy for Severe Pelvic Organ Prolapse

Start date: January 2016
Phase: N/A
Study type: Interventional

This prospective randomized pilot study is aimed to verify if the operative time of a standard laparoscopic sacral colpopexy associated to subtotal hysterectomy for the treatment of POP could be further reduced using a continuous locked suture vs. conventional single 5-points suture for anterior mesh fixation.

NCT ID: NCT03421457 Completed - Clinical trials for Pelvic Organ Prolapse

Laparoscopic Lateral Suspension With Mesh & Sacrocervicopexy for the Treatment of Uterine Prolapse

Start date: January 24, 2018
Phase: N/A
Study type: Interventional

This study is aimed to compare the efficiency of two uterus-preserving laparoscopic methods to treat uterine prolapse in a randomized controlled trial. Laparoscopic lateral suspension with mesh (LLSM) will be compared with laparoscopic sacrohysteropexy (LS). Both procedures are known as sufficient uterus preserving methods. LLSM was introduced to be an alternative to others with avoiding dissection of promontory and therefore being safer, faster and feasible technique.

NCT ID: NCT03421067 Completed - Clinical trials for Pelvic Organ Prolapse

Apical Support During Hysterectomy for Pelvic Organ Prolapse-NSQIP Analysis.

Start date: February 27, 2018
Phase:
Study type: Observational

This is a retrospective descriptive study using the American College of Surgeon's National Surgical Quality Improvement Program® (ACS NSQIP®) data to determine whether gynecologic surgeons are already meeting the recently recommended best practice of supporting the vaginal apex at time of hysterectomy for pelvic organ prolapse (POP).

NCT ID: NCT03387202 Completed - Clinical trials for Pelvic Organ Prolapse

Laparoscopic Lateral Mesh Suspension for Pelvic Organ Prolapse

Start date: November 1, 2016
Phase: N/A
Study type: Observational [Patient Registry]

This study is aimed to share our clinical experience in an uterine-preserving laparoscopic lateral suspension of apical prolapses with mesh operation after minor modifications in technique. Transperineal ultrasonography and several questionnaires are used for objective and subjective outcomes.

NCT ID: NCT03379246 Completed - Clinical trials for Pelvic Organ Prolapse

Apical Support During Hysterectomy for Pelvic Organ Prolapse

Start date: December 5, 2017
Phase:
Study type: Observational

This is a retrospective chart review using TriHealth Electronic Privacy Identification Center (EPIC) to determine whether gynecologic surgeons at a large community hospital are already meeting the recently recommended best practice of supporting the vaginal apex.

NCT ID: NCT03378622 Active, not recruiting - Clinical trials for Pelvic Organ Prolapse

Anchor for Robotic Sacrocolpopexy

ARiSe
Start date: November 29, 2017
Phase: Phase 3
Study type: Interventional

1. PRIMARY OBJECTIVE: To assess the effect of absorbable anchor compared to suturing for mesh attachment to vagina in robotic assisted sacrocolpopexy on the length of surgery for this portion of the procedure. 2. SECONDARY OBJECTIVES: i. To assess intraoperative and ii. postoperative complication rates, iii. Intraoperative 10 cm visual analog scale (VAS), to subjectively assess surgeon satisfaction with the technique iv. post-operative Pelvic Organ Prolapse Quantification (POPQ) evaluation for anatomic failure and v. a VAS of the vaginal walls overall appearance

NCT ID: NCT03349736 Completed - Clinical trials for Urinary Incontinence

Pelvic Floor Muscle Training Programme in Pregnant Nepalese Women- a Feasibility Study

PFMT
Start date: June 25, 2017
Phase: N/A
Study type: Interventional

To our knowledge, no studies in Nepal have reported the feasibility of performing the pelvic floor muscle training in Nepalese women. The aim of the study is to develop and a pelvic floor muscle training programme based on information, education (leaflet, video) and pelvic floor muscles (PFM) exercise in order to prevent or reduce Pelvic organ prolapse(POP) and Urinary Incontinence (UI) in pregnant Nepalese women. The women will receive information (leaflet, video, posters) and guidance on PFMT. Following this, the women are advised to perform daily home PFM exercise Women will record their home PFMT using an exercise diary.

NCT ID: NCT03315715 Completed - Clinical trials for Pelvic Organ Prolapse

Dynamic Magnetic Resonance Imaging Before and After Vaginal Prolapse Repair

Start date: March 1, 2018
Phase:
Study type: Observational

This study is to describe the impact of vaginal reconstruction, including an intraperitoneal vaginal vault suspension for pelvic organ prolapse (POP) on pelvic anatomy using dynamic magnetic resonance imaging (MRI) of the pelvis.