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Anterior Pelvic Prolapse Reconstruction With TiLOOP® Total 6

NCT01084889 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 292

Last updated 2019-02-04

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 titanised polypropylene mesh on rate of erosion and patients quality of live.

Conditions

  • Cystocele
  • Uterine Prolapse

Interventions

DEVICE

surgical mesh implantation (TiLOOP® Total 6)

The standard procedure for the surgical repair of anterior prolapse is via the obturator membrane. The surgical mesh TiLOOP® Total 6 is placed transvaginal by the aid of TiLOOP® surgical instruments to place the mesh arms.

Sponsors & Collaborators

  • Aix Scientifics

    collaborator INDUSTRY

  • GfE Medizintechnik GmbH

    collaborator OTHER

  • pfm medical titanium gmbh

    collaborator UNKNOWN

  • Bayes GmbH

    collaborator OTHER

  • Crolll Gmbh

    collaborator OTHER

  • pfm medical gmbh

    lead INDUSTRY

Principal Investigators

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

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2014-01-31
Completion
2016-06-30

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 NCT01084889 on ClinicalTrials.gov