Safety and Performance of the EndoFast Reliant SCP in Vaginal Wall Reinforcement

NCT03516136 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 84

Last updated 2018-05-17

No results posted yet for this study

Summary

A Single arm, single site, retrospective cohort Post Marketing Clinical Follow up Study Evaluating the Safety and Performance of the EndoFast Reliant SCP for apical support.

Conditions

  • Pelvic Organ Prolapse

Interventions

DEVICE

EndoFast Reliant SCP

POP repair procedure with the EndoFast Reliant SCP system

Sponsors & Collaborators

  • Allium, Ltd.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-01
Primary Completion
2017-12-31
Completion
2017-12-31

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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 NCT03516136 on ClinicalTrials.gov