Actively Recruiting
Trial to Evaluate Fecobionics in Fecal Incontinence (FI) (NORMAL and ABNORMAL-FI)
Led by The California Medical Innovations Institute, Inc. · Updated on 2025-10-21
155
Participants Needed
2
Research Sites
215 weeks
Total Duration
On this page
Sponsors
T
The California Medical Innovations Institute, Inc.
Lead Sponsor
A
Augusta University Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
The objective is to determine the length-tension properties of the anal sphincters using Fecobionics in normal subjects and FI patients during anal distension and during simulated evacuation. Fecobionics has the consistency and shape of normal stool and can record pressures, cross-sectional area, orientation and viscoelastic properties of the anorectum and can map the geometric profiles during evacuation, and thereby provides multi-dimensional measurements of pressures, deformability, and topographic changes. Fecobionics combines several existing tests to provide novel insight into anorectal function. The purpose for the development was to overcome the technological controversies and disagreement between various tests and unphysiological test conditions. The aim was to imitate defecation as much as possible to the natural process. Fecobionics was developed to simulate stool and to provide the driving pressure and resulting deformations of stool along with a measure of an objective anorectal angle during defecation in a single examination. Fecobionics makes it possible to describe objectively, without disturbing the defecation process, the opening characteristics and pressure signatures during initial entry into the relaxing anal canal. The overall goal is to provide mechanistic understanding of defecation in health and defecatory disorders. It exceeds previous attempts to make artificial stool for evaluation of defecation (BET and FECOM) and integrates other technologies as well. It was designed to have a consistency and deformability of Type 4 (range type 3-5) on the Bristol stool form scale. The range from types 3-5 is found in 70% of normal subjects. A major novelty is that Fecobionics measures pressures in axial direction; i.e., in the flow direction.
CONDITIONS
Official Title
Trial to Evaluate Fecobionics in Fecal Incontinence (FI) (NORMAL and ABNORMAL-FI)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subject must provide written informed consent
- Willing and able to undergo required study tests, surveys, and procedures
- Age > 18 years of age
You will not qualify if you...
- Female who is pregnant
- Prior anorectal surgery
- Prior bowel resection
- History of chronic constipation
- In the opinion of the investigator, the subject is not a suitable candidate for the study
AI-Screening
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Trial Site Locations
Total: 2 locations
1
California Medical Innovations Institute
San Diego, California, United States, 92121
Active, Not Recruiting
2
Augusta University Medical Center
Augusta, Georgia, United States, 30912
Actively Recruiting
Research Team
H
Hans Gregersen, MD, PhD
CONTACT
S
Satish Rao, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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