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Anterior Pelvic Prolapse Reconstruction With TiLOOP® PRO A Polypropylene Mesh

NCT02690220 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2019-10-23

No results posted yet for this study

Summary

The purpose of this study is to determine the influence of anterior pelvic prolapse reconstruction with a titanized polypropylene mesh on patients quality of life.

Conditions

  • Cystocele
  • Uterine Prolapse

Interventions

DEVICE

TiLOOP® PRO Plus A

The standard operation method for the surgical repair of anterior prolapse is via the obturator membrane. The mesh is placed trans-vaginally using the TiLOOP® Application Set to place the mesh arms.

Sponsors & Collaborators

  • Crolll Gmbh

    collaborator OTHER

  • Bayes GmbH

    collaborator OTHER

  • Aix Scientifics

    collaborator INDUSTRY

  • pfm medical gmbh

    lead INDUSTRY

Principal Investigators

  • Christian Fünfgeld, Dr. med. · Klinik Tettnang GmbH

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-01
Primary Completion
2017-07-31
Completion
2017-07-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02690220 on ClinicalTrials.gov