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

A

Allium

Status

Completed

Conditions

Pelvic Organ Prolapse

Treatments

Device: EndoFast Reliant SCP

Study type

Observational

Funder types

Industry

Identifiers

NCT03516136
CL-SCP-60-04-R

Details and patient eligibility

About

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.

Enrollment

84 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Female subjects >18 years old that underwent Pelvic Organ Prolapse repair utilizing the EndoFast Reliant SCP

Exclusion criteria

  1. Patients without follow-up

Trial design

Trial documents
1

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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