Clinical Trials Logo
  1. Home
  2. Vaginal Prolapse
  3. NCT00196495

Clinical Assessment of the Total Vaginal Mesh Technique for Treatment of Genital Prolapse

Vaginal Prolapse Clinical Trial

Official title:
Clinical Assessment of the Total Vaginal Mesh Technique for Treatment of Genital Prolapse

Clinical Trial Summary

Pelvic floor prolapse is a general term used to describe various clinical conditions that are associated with pelvic floor (muscles that support the vagina) relaxation in female patients.Pelvic floor prolapse is thought to result from a stretching, weakening or tearing of the soft tissue structures that support the pelvic organs. These tissues become compromised because of a weakened or damaged.The purpose of the study will be to demonstrate the usability of Polypropylene Mesh for prolapse repair, using the TVM technique.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00196495
Study type Interventional
Source Ethicon, Inc.
Contact
Status Completed
Phase Phase 4
Start date June 2004
Completion date November 2005
View Details
See also
  Status Clinical Trial Phase
Recruiting NCT04701047 - Prospective Observational Prolapse Study
Recruiting NCT03664986 - Pudendal Block Using Liposomal Bupivacaine vs. Standard Treatment During Sacrospinous Ligament Fixation Phase 4
Completed NCT00388947 - Observational Data Collection of Surgical Outcomes in the Treatment of Vaginal Prolapse With AMS Products N/A
Active, not recruiting NCT00442247 - A Randomised, Controlled Study of Bimesh, Pelvicol for Vaginal Wall Prolapse N/A
Not yet recruiting NCT04078802 - 0050-19-RMB CTIL - VNOTES Compared to VH for Vaginal Apex Prolapse N/A
Recruiting NCT00918099 - The Use of Avaulta for Anterior Repair N/A
Completed NCT00769054 - Local Infiltration Analgesia With Ropivacaine in Posterior Vaginal Wall Prolapse:a Randomized, Double-Blind Study Phase 4
Completed NCT03187574 - Comparison of Two Vaginal Mesh Kits in the Management of Vaginal Prolapse N/A
Completed NCT00679276 - Treatment Outcomes of Vaginal Prolapse Repair N/A
Completed NCT03338400 - Dexamethasone Administration To Improve Patient Recovery In Ambulatory Vaginal Prolapse Surgery: Is There A Role? Phase 2
Completed NCT00153231 - Posterior IVS Versus Sacrospinous Suspension in Vaginal Vault Prolapse Repair Phase 4
Completed NCT01409902 - Using a Sheathed Speculum to Visualize and Access the Cervix In Women With Excessive Vaginal Tissue N/A
Completed NCT00557882 - Efficacy Study of Vaginal Mesh for Anterior Prolapse Phase 4
Not yet recruiting NCT06234449 - The Impact of Long-term Pessary Use on Pelvic Organ Prolapse oìduring Covid-19 Pandemic in Patients Attending Surgery
Active, not recruiting NCT03658395 - Sacrocolpopexy With Posterior Repair Obstructed Defecation Symptoms N/A
Recruiting NCT05449054 - Continuous Stitches Versus Simple Interrupted Stitches for Anterior Colporrhaphy N/A
Completed NCT00475540 - Efficacy Study of Vaginal Mesh for Prolapse N/A
Enrolling by invitation NCT00571350 - Anterior Vaginal Wall Reconstruction Phase 1/Phase 2
Not yet recruiting NCT03333811 - Sexual Function After Vaginal Repair With Perineorrhaphy N/A
Completed NCT02431897 - Investigation to Minimize Prolapse Recurrence of the Vagina Using Estrogen Phase 4