Retrospective Data Analysis PelviGYNious/EndoGYNious

NCT06927752 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2025-04-15

No results posted yet for this study

Summary

The retrospective patient chart review aims to generate additional data to substantiate the safety and performance of EndoGYNious and PelviGYNious.

Conditions

  • Prolapse
  • Sacrocolpopexy
  • Pelvic Organ Prolapse (POP)

Interventions

DEVICE

PelviGYNious

Patient received PelviGYNious implant.

DEVICE

EndoGYNious

Patient received EndoGYNious implant.

Sponsors & Collaborators

  • A.M.I. Agency for Medical Innovations GmbH

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-01
Primary Completion
2025-05-31
Completion
2025-08-31

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 NCT06927752 on ClinicalTrials.gov