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Severity of Fecal Incontinence and Manometric Values Using the Anopress® Device in Women — MANOPRESS  

Fecal Incontinence Clinical Trial

Official title:
Severity of Fecal Incontinence and Manometric Values Using the Anopress® Device in Women

Clinical Trial Summary

The purpose of this study is to stablish a correlation between fecal incontinence severity scales (Wexner & St. Mark's) and manometric values obtained using the Anopress® portable manometry and values obtained using endoanal ultrasound in women with fecal incontinence.

Clinical Trial Description

The Anopress® portable anal manometry will be used to measure the pressures of the anal canal in different phases: rest, squeeze, strain and endurance. All female patients referred with the diagnosis of fecal incontinence giving written informed consent will undergo a endoanal portable manometry at our outpatients clinics. They will be asked to fill out the severity questionaries (Sant Mark's and Wexner). All data will be collected for analysis. An endoanal ultrasound will be performed in all patients to assess the sphincter integrity. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05058326
Study type Observational [Patient Registry]
Source Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta
Contact
Status Completed
Phase
Start date September 20, 2020
Completion date October 1, 2021
View Details
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