Vaginal Prolapse
Conditions
Keywords
Vagina, Prolapse, Anterior vaginal wall prolapse
Brief summary
Pelvic organ prolapse is characterized by a lack of pelvic floor support causing the pelvic organs and vaginal walls to protrude. For decades, suture repair techniques have been the primary choice of surgical treatment when indicated. Traditional surgical techniques are frequently associated with unsatisfying anatomical recurrence rates and it is plausible that inherently weak, or damaged, pelvic floor supportive tissues need to be reinforced by a permanent support to avoid the high rates of recurrences commonly described using traditional techniques. Over the years sporadic attempts have been made to introduce novel surgical techniques using a variety of biomaterials with varying success. Despite a lack of clinical safety data, or compelling clinical evidence demonstrating that it improves outcomes compared to traditional suture techniques, use of biomaterials in pelvic reconstructive surgery has become widespread in just a few years . It is likely that biomaterials need to be anchored in tissues not afflicted by the disease, in order to provide the intended pelvic floor support. This has given rise to transvaginal surgical techniques using a transobturator approach passing the mesh through the arcus tendineous fascia pelvis, or the sacrospinous ligaments through a transgluteal approach. Short term data from concluded and on-going safety assessments of these techniques has provided promising results and satisfying clinical outcomes. The aim of the present study is to compare anterior mesh repair (PROLIFT®) with traditional suture repair in a randomised trial.
Interventions
Standardised colporrhaphy of the anterior vaginal wall
Transvaginal mesh surgery of the anterior vaginal wall
Sponsors
Study design
Eligibility
Inclusion criteria
* Reproductive years in the past (biologically or reproductive decision) * Prolapse of the anterior vaginal wall ≥POPQ-stadium II * Prolapse specific pelvic symptom * Being able to make an informed consent on participation * Physically and cognitive capable of participating in the required follow-up * No other pelvic floor surgery performed at the time of anterior repair * No
Exclusion criteria
fulfilled
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Combined primary outcome measure: anatomical assessment according to the pelvic organ prolapse quantification system and prolapse specific symptom | One year |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life | One year |
Countries
Denmark, Finland, Norway, Sweden