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Comparison Between Transvaginal Mesh and Traditional Surgery for Pelvic Organ Prolapse

A Randomised Controlled Trial of Transvaginal Mesh (PROLIFT) Versus Anterior Colporrhaphy in Anterior Vaginal Wall Prolapse

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00566917
Enrollment
400
Registered
2007-12-04
Start date
2007-12-31
Completion date
2010-01-31
Last updated
2010-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vaginal Prolapse

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

PROCEDUREAnterior PROLIFT

Transvaginal mesh surgery of the anterior vaginal wall

Sponsors

The regional agreement on medical training and clinical research (ALF) between Stockholm county council and Karolinska Institutet.
CollaboratorUNKNOWN
The Swedish Society of Medicine
CollaboratorOTHER
Investigators meetings supported by Gynecare Scandinavia.
CollaboratorUNKNOWN
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frame
Combined primary outcome measure: anatomical assessment according to the pelvic organ prolapse quantification system and prolapse specific symptomOne year

Secondary

MeasureTime frame
Quality of lifeOne year

Countries

Denmark, Finland, Norway, Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026