FENIX™ Continence Restoration System Registry

Status Completed

Clinical Trial Summary

The FENIX Registry is a multi-center, observational database designed to collect data regarding the FENIX™ Continence Restoration System in everyday clinical practice, evaluate the clinical course of patients from pre-operative assessment through five years post-surgery and Track and monitor effectiveness and safety through the use of a bowel diary, fecal incontinence quality-of-life measures and adverse event reporting. Up to 25 sites will participate in the Registry. Sites to enroll consecutive eligible patients into the Registry. Registry will enroll approximately 200 FENIX patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04007250
Study type	Observational [Patient Registry]
Source	Torax Medical Incorporated
Contact
Status	Completed
Phase
Start date	January 7, 2012
Completion date	February 27, 2019

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