Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
94 participants
OBSERVATIONAL
2012-01-07
2019-02-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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FENIX participants
Individuals being treated with the FENIX™ Continence Restoration System.
FENIX™ Continence Restoration System
The FENIX™ Continence Restoration System is indicated for use for the treatment of chronic fecal incontinence in patients who have failed or are not candidates for more conservative therapy. The FENIX™ System Implant is placed around the external anal sphincter to augment a weak anal sphincter and restore continence.
The FENIX™ System is comprised of the following components:
* FENIX™ System Implant
* FENIX™ System Anal Sphincter Sizing Tool The FENIX™ System Implant consists of a series of titanium beads with magnetic cores that are connected with independent titanium wires to form an annular shape. The attractive force of the magnetic beads is designed to provide additional strength to keep a weak anal sphincter closed.
Interventions
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FENIX™ Continence Restoration System
The FENIX™ Continence Restoration System is indicated for use for the treatment of chronic fecal incontinence in patients who have failed or are not candidates for more conservative therapy. The FENIX™ System Implant is placed around the external anal sphincter to augment a weak anal sphincter and restore continence.
The FENIX™ System is comprised of the following components:
* FENIX™ System Implant
* FENIX™ System Anal Sphincter Sizing Tool The FENIX™ System Implant consists of a series of titanium beads with magnetic cores that are connected with independent titanium wires to form an annular shape. The attractive force of the magnetic beads is designed to provide additional strength to keep a weak anal sphincter closed.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Individuals who have provided appropriate authorization per institutional policy and procedure to have clinical and health information collected for the FENIX Registry.
* Individuals willing to complete a 14-day bowel diary, questionnaires and comply with all required follow-up.
Exclusion Criteria
ALL
No
Sponsors
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Torax Medical Incorporated
INDUSTRY
Responsible Party
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Locations
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University Hospital of Nantes
Nantes, , France
Kliniken Essen-Mitte
Essen, , Germany
Countries
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Other Identifiers
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3422
Identifier Type: -
Identifier Source: org_study_id
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