SphinkeeperTM Procedure for Treating Severe Faecal Incontinence
Study Details
Study Description
Brief Summary
Patients, aged 18 - 90 years, undergoing sphinkeeper operation at the Department of General Surgery at the Medical University of Vienna are enrolled into our study. Primary endpoints is the functional outcome as well as movement, migration and extrusion of sphinkeeper prostheses after implantation by endoluminal ultrasound and manometrical examination.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
The Sphinkeeper™ implantation for fecal incontinence is a novel surgical procedure with limited data on its clinical efficacy. Therefore, we aimed to assess the functional outcome following Sphinkeeper™ surgery in patients with refractory FI.
Patients with FI, who met the inclusion criteria were enrolled to our study and received Sphinkeeper™ implantation. Functional outcome and quality of life was evaluated by standard questionnaires before and after surgery. In the routine check-up patients received endoanal ultrasound and anorectal manometry.
Study Design
Outcome Measures
Primary Outcome Measures
- Faecal incontinence assessment [six months]
Episodes and number of faecal incomtinence and stool form with faecal incontinence were assessed using the Vaizey incontinence score (range 0-22, higher numbers mean severe incontinence forms)
Secondary Outcome Measures
- Psychological und physical well-being [six months]
The Psychological und physical well-being before and after implantation of Sphinkeeper was assessed using the SF12 standardized questionnaire (range 0-100; higher scores= Better quality of life)
- Migration of Sphinkeeper prostheses [six months]
The Migration of Sphinkeeper prostheses were analyzed using endoanal ultrasound one and six months after implantation. The prostheses will be categorized by their position in relation to the anal canal axis. (Grade of rotation to the anal canal axis)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age 18 - 90 years, undergoing sphinkeeper operation at the Department of General Surgery, Medical University of Vienna
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Ability and willingness to understand and comply with study interventions and restrictions.
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Voluntarily signed informed consent after full explanation of the study to the participant.
Exclusion Criteria:
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Any physical or mental disorder, which could interfere with the participant's safety during the clinical trial or with the study objectives
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Inability to communicate well with the investigator due to language problems or reduced mental development
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Inability or unwillingness to give written informed consent
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Medical University of Vienna | Vienna | Austria | 1090 |
Sponsors and Collaborators
- Medical University of Vienna
Investigators
- Study Chair: Stefan Riss, Prof.MD, Medical University of Vienna, Head of Pelvic Floor surgery
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2338/2019