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Fecobionics in Biofeedback Therapy in Dyssynergia Patients

Primary Purpose

Dyssynergia, Constipation

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Fecobionics
Sponsored by
The California Medical Innovations Institute, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Dyssynergia focused on measuring Fecobionics, Biofeedback therapy, Defecation

Eligibility Criteria

21 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subject must provide written informed consent. Age between 21-75 years. Subjects must fulfill the criteria for obstructed defecation/dyssynergia and enter the BFT at UCSD or Scripps. Exclusion Criteria: Female who is pregnant or lactating. Prior abdominal or anorectal surgery or bowel resection. Diagnosis of fecal incontinence, any anorectal symptoms and drug use that affect anorectal function. Confirmed or suspected COVID-19 infection. Severe cardiovascular disease. Subjects not willing to consent and undergo the specified tests in this study. Other exclusions, that in the opinion of the investigator, the volunteer is not a suitable subject for the study.

Sites / Locations

  • California Medical Innovations Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Fecobionics

Arm Description

Outcomes

Primary Outcome Measures

Expulsion Duration
The time it takes to defecate Fecobionics
Pressure Difference between front and rear ends of Fecobionics
A measure of anal sphincter pressure, the driving rectal pressure, and the difference between these two pressures. This is the key to the determination of defecation phases.

Secondary Outcome Measures

Anorectal angle
Anorectal angle is an important parameter for defecation
Mechanical Tension of Fecobionics
To reflect anorectal function, the mechanical tension will be computed. The tension is equal to anorectal radius multiply pressure.
Expulsion Velocity
Measured from the time difference between multiple sensor data
Cross-sectional area
Computed by diameter

Full Information

First Posted
March 16, 2023
Last Updated
July 3, 2023
Sponsor
The California Medical Innovations Institute, Inc.
Collaborators
Scripps Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT05807321
Brief Title
Fecobionics in Biofeedback Therapy in Dyssynergia Patients
Official Title
Fecobionics to Monitor and Predict Biofeedback Therapy in Dyssynergia Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 15, 2023 (Anticipated)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
March 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The California Medical Innovations Institute, Inc.
Collaborators
Scripps Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Constipation affects 12-19% of Americans. Pelvic floor dyssynergia is considered to play an important role in constipation but the underlying mechanisms are not well understood in individual patients. The investigators have developed a novel device named Fecobionics that provide detailed mapping of physiological parameters during defecation. The aim of the study is to use Fecobionics to assess anorectal function in dyssynergia patients and monitor and predict the outcome of the biofeedback therapy.
Detailed Description
This study aims to monitor and predict biofeedback therapy based on mechanism-based and highly integrated data using a new medical device. This study is specifically for patients with dyssynergia before, during, and after biofeedback therapy. The balloon-like Fecobionics device (10 cm long and 1 cm in diameter) will be inserted into the participant's rectum and will record data before and during the expulsion of the device. The participant will be asked to do different motions like cough, squeeze, or push during the procedure. The novel data obtained in this study may help the investigators to identify the patients who will benefit or not benefit from biofeedback therapy before the therapy is done. This will determine the effectiveness of treatments for anorectal disorders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyssynergia, Constipation
Keywords
Fecobionics, Biofeedback therapy, Defecation

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fecobionics
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Fecobionics
Other Intervention Name(s)
Anorectal manometry, Balloon expulsive test
Intervention Description
Fecobionics is a novel device to be inserted through the anal canal into rectum for studying defecation. Anorectal manometry and balloon expulsion test may be used as reference. Anorectal manometry and balloon expulsive test are standard methods for anorectal functional measurement.
Primary Outcome Measure Information:
Title
Expulsion Duration
Description
The time it takes to defecate Fecobionics
Time Frame
1.5 year
Title
Pressure Difference between front and rear ends of Fecobionics
Description
A measure of anal sphincter pressure, the driving rectal pressure, and the difference between these two pressures. This is the key to the determination of defecation phases.
Time Frame
1.5 year
Secondary Outcome Measure Information:
Title
Anorectal angle
Description
Anorectal angle is an important parameter for defecation
Time Frame
1.5 year
Title
Mechanical Tension of Fecobionics
Description
To reflect anorectal function, the mechanical tension will be computed. The tension is equal to anorectal radius multiply pressure.
Time Frame
1.5 year
Title
Expulsion Velocity
Description
Measured from the time difference between multiple sensor data
Time Frame
1.5 year
Title
Cross-sectional area
Description
Computed by diameter
Time Frame
1.5 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject must provide written informed consent. Age between 21-75 years. Subjects must fulfill the criteria for obstructed defecation/dyssynergia and enter the BFT at UCSD or Scripps. Exclusion Criteria: Female who is pregnant or lactating. Prior abdominal or anorectal surgery or bowel resection. Diagnosis of fecal incontinence, any anorectal symptoms and drug use that affect anorectal function. Confirmed or suspected COVID-19 infection. Severe cardiovascular disease. Subjects not willing to consent and undergo the specified tests in this study. Other exclusions, that in the opinion of the investigator, the volunteer is not a suitable subject for the study.
Facility Information:
Facility Name
California Medical Innovations Institute
City
San Diego
State/Province
California
ZIP/Postal Code
92121
Country
United States

12. IPD Sharing Statement

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Fecobionics in Biofeedback Therapy in Dyssynergia Patients

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