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Prolapse clinical trials

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NCT ID: NCT03715803 Completed - Clinical trials for Pelvic Organ Prolapse

Calistar A vs. Calistar S - Comparative Cohort Retrospective Analysis of Single Incision POP Systems

Start date: October 25, 2018
Phase:
Study type: Observational

The main objective of this study is to compare the initial outcomes and complication of two meshes implanted through a single incision to treat anterior and apical prolapses, Calistar A and a second-generation low weight mesh called Calistar S (Soft).

NCT ID: NCT03706716 Completed - Clinical trials for Pelvic Organ Prolapse

Testing a Decision Aid for Women With Urogenital Prolapse

Start date: June 7, 2018
Phase: N/A
Study type: Interventional

Development of a decision aid for women with urogenital prolapse followed by an intervention with use of the decision aid to investigate the effect on the perceived shared decision making in the clinical consultations. A protocol for a randomized controlled non blinded multicenter trial. A feasibility trial for the protocol.

NCT ID: NCT03681223 Completed - Clinical trials for Vaginal Vault Prolapse

Restorelle® Y Mesh vs. Vertessa® Lite Y Mesh for Laparoscopic and Robotic-assisted Laparoscopic Sacrocolpopexy

Lite-Y
Start date: September 18, 2018
Phase: N/A
Study type: Interventional

This is a randomized clinical trial to compare outcomes between the Restorelle® Y mesh and Vertessa® lite Y mesh for the treatment of vaginal vault prolapse. Hypothesis: Vertessa® lite Y mesh is not inferior to Restorelle® Y mesh for the treatment of vaginal vault prolapse

NCT ID: NCT03643393 Completed - Rectal Prolapse Clinical Trials

Report 2 Cases of Massive Incarceration Necrosis Rectal Prolapse Are Successfully Treated With Altemeier's Procedure

Start date: May 1, 2015
Phase: N/A
Study type: Interventional

Incarceration and necrosis of rectal prolapse is rare and often requires urgent management. Perineal rectosigmoidectomy (Altemeir procedure) is a reasonable technique for this condition. The need for a diverting stoma depends on the patient's condition and the experience and judgement of the surgeon. A literature review was performed to determine optimal management of incarcerated and necrotic rectal prolapse, and to determine the indication for fecal diversion.

NCT ID: NCT03642054 Completed - Clinical trials for Pelvic Organ Prolapse

Advanced Biomarker Assessment in Pelvic Organ Prolapse

Start date: June 29, 2018
Phase:
Study type: Observational

This study will assess advanced biomarkers in patients with and without vaginal prolapse. Assessments will be directed at vaginal fibroblasts and adipose derived stem cells.

NCT ID: NCT03634878 Completed - Clinical trials for Prolapse of the Uterus

Evaluation of the Position of Promontofixation Prostheses in Perineal Ultrasound

PROMONOTECHO
Start date: April 2016
Phase: N/A
Study type: Interventional

Indirect promontofixation with prostheses is the standard surgical technique for the reference of uterine prolapse. There is no validated examination to control the position of the prostheses postoperatively. These prostheses are echogenic and perineal ultrasound could be a means of postoperative monitoring. There is no data in the literature on the relationship between prosthesis position and postoperative symptoms

NCT ID: NCT03624764 Completed - Prolapse Clinical Trials

Assisted Promontofixation Using Glue Versus Promontofixation Using Threads (PROCOL)

PROCOL
Start date: January 4, 2017
Phase: N/A
Study type: Interventional

The treatment of gynecological prolapse (organ removal) can be done by laparoscopy or vaginally. Laparoscopy is used in 1 out of 2 cases, but learning is difficult and operation time is long. One of the technical difficulties is related to the sutures to the threads. Some surgeons therefore use a glue to fix prosthetic reinforcements more easily and quickly, but this sizing technique has only been evaluated very little. Our study proposes to compare the technique of suture with the thread at the gluing of the prostheses in order to validate the merits of this new technique

NCT ID: NCT03609229 Completed - Prolapse Clinical Trials

Outcomes After Sacrocolpopexy With and Without Burch to Prevent Stress Urinary Incontinence in 3rd and 4th Degree Apical Uterine Prolapse

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Urinary incontinence will develop after prolapse repair in approximately one quarter of patients with advanced pelvic organ prolapse who remain continent despite significant loss of anterior vaginal and pelvic organ support. Many women with advanced pelvic organ prolapse who choose to undergo surgical management also choose to undergo continence surgery in order to prevent new onset urinary incontinence.

NCT ID: NCT03607344 Completed - Clinical trials for Pelvic Organ Prolapse

Day Case Laparoscopic Sacrocolpopexy, a New Management

Start date: January 1, 2016
Phase:
Study type: Observational

Facing the stakes of hospital beds, this study assessed day case variant technic of laparoscopic sacrocolpopexy with or without robotic assistant.

NCT ID: NCT03586219 Completed - Clinical trials for Pelvic Organ Prolapse

Postoperative Opioid Consumption After Urogyneocologic Surgery

Start date: December 29, 2017
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled trial is to evaluate whether preoperative opioid education will reduce postoperative opioid consumption after urogynecologic surgeries. Additionally, the effect of the opioid education on opioid storage and disposal patterns will be evaluated. The pattern of opioid consumption 2 and 6 weeks after surgery will be compared between patients in the study arms. The rates of prescription refills 12 weeks and 12 months after the surgery will be compared between patients in the study arms.