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Studies in Patients With Defecatory Disorders

Primary Purpose

Fecal Incontinence, Constipation

Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Fecobionics
Sponsored by
Giome
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Fecal Incontinence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy subjects: Asymptomatic healthy persons aged over 18 years who can give informed consent.
  • CC (Chronic Constipation) Patients: Patients over 18 with history of FI for over 3months, who are able to give consent.
  • FI (Fecal Incontinence) patients: Patients over 18 with history of FI for over 3months, who are able to give consent.
  • Patients with a stoma who are over 18 years and able to give consent.

Exclusion Criteria:

  • Healthy subjects: Persons with a history of constipation or fecal incontinence, prior abdominal surgery, medication, and diseases, especially chronic diseases that affect bowel function and defecation. Pregnant women will also be excluded.
  • CC Patients: Patients, who are not willing to undergo the proposed test program and patients with prior anorectal or intestinal surgery. Pregnant women and patients with chronic dehydration and on medications like opioids will also be excluded.
  • FI patients: 1) Patients who are not willing to undergo the specified tests in this study, 2) Pregnant women and 3) Patients who has had anorectal surgery or bowel resection.
  • Patients with stoma: Patients, who are not willing to undergo the proposed test program and patients who have inflammation or symptoms related to the stoma.

Sites / Locations

  • Prince of Wales HospitalRecruiting
  • Department of Surgery, Prince of Wales HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Fecobionics studies

Arm Description

Outcomes

Primary Outcome Measures

Decreased anorectal pressure assessed with the Fecobionics device
The number of participants with low anorectal pressure during defecation

Secondary Outcome Measures

Decreased anorectal mechanical stress assessed with the Fecobionics device
The number of participants with low anorectal mechanical stress during defecation
Decreased anorectal angle assessed with the Fecobionics device
The number of participants with small anorectal angle during defecation
Wave-like decrease in cross-sectional area with the Fecobionics device
The amount of recordings with retrograde intestinal ripples

Full Information

First Posted
October 3, 2017
Last Updated
March 1, 2021
Sponsor
Giome
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1. Study Identification

Unique Protocol Identification Number
NCT03317938
Brief Title
Studies in Patients With Defecatory Disorders
Official Title
Unraveling Anorectal Function and Biomarker Signatures in Patients Suffering From Subtypes of Defecatory Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Recruiting
Study Start Date
August 14, 2017 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Giome

4. Oversight

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

5. Study Description

Brief Summary
Defecatory disorders like chronic constipation and faecal incontinence affect 25% of the population with rising incidence. Defecatory disorders pose a major health care burden and are poorly recognized and treated. The need for better diagnostics and therapeutics is substantial. Current assessment of patients with constipation and faecal incontinence include endoscopic assessment to rule out intraluminal organic cause for patients' symptoms, endoanal ultrasound scan / MRI to assess patients' pelvic floor anatomy and anorectal manometry and balloon expulsion test to assess anorectal function. All tests are susceptible to measurement artifacts. The standard technologies for anorectal assessment are anorectal manometry, balloon expulsion test and defecography. Endoluminal Functional Lumen Imaging Probe (EndoFLIP©) is a novel technology, originally used to measure the dimensions and function of a hollow organ. Anorectal manometry, balloon expulsion test, defecography, and the EndoFLIP probe will be used in the proposed studies. In addition, the proposed study intends to use a simulated feces named Fecobionics which is a device that integrates several technologies into one which will save time and reduce test variability. In the proposed studies investigators will assess defecatory function in subgroups of Hong Kong patients suffering from chronic constipation and faecal incontinence and determine biomarkers to increase the diagnostic value of anorectal testing. Investigators will study up to 130 patients with anorectal disorders and 101 healthy control subjects. Investigators anticipate to improve diagnostics of anorectal disorders considerably and to learn about physiological mechanisms that affect defecatory efficacy.
Detailed Description
Defecatory disorders like chronic constipation and faecal incontinence affect 25% of the population with rising incidence. Defecatory disorders pose a major health care burden and are poorly recognized and treated. The need for better diagnostics and therapeutics is substantial. Currently management options for these patients are limited, partly due to the fact that control of defaecation and continence is multifactorial but also due to the fact that it is difficult to identify the exact cause of patients' incontinence. Even in healthy subjects, many aspects of defecatory mechanisms are yet not well understood. Current assessment of patients with constipation and faecal incontinence include endoscopic assessment to rule out intraluminal organic cause for patients' symptoms, endoanal ultrasound scan / MRI to assess patients' pelvic floor anatomy and anorectal manometry and balloon expulsion test to assess anorectal function. All tests are susceptible to measurement artifacts, with a high inter-individual variation with significant overlap between healthy asymptomatic and symptomatic patients. The standard technologies for anorectal assessment are anorectal manometry, ballon expulsion test and defecography. Endoluminal Functional Lumen Imaging Probe (EndoFLIP©) is a novel technology, originally used to measure the dimensions and function of a hollow organ. Anorectal manometry, balloon expulsion test, defecography, and the EndoFLIP probe will be used in the proposed studies. In addition, the proposed study intends to use a simulated feces named Fecobionics which is a device that integrates several technologies into one which will save time and reduce test variability. A major difference from EndoFLIP and other technologies like anorectal manometry is that the device will be defecated rather than providing static data from one location in the anal canal. In the proposed studies investigators will assess defecatory function in subgroups of Hong Kong patients suffering from chronic constipation and faecal incontinence and determine biomarkers to increase the diagnostic value of anorectal testing. Investigators will study up to 130 patients with anorectal disorders and 101 healthy control subjects. Investigators anticipate to improve diagnostics of anorectal disorders considerably and to learn about physiological mechanisms that affect defecatory efficacy. For example, one substudy investigates the effect of posture on defecation and another substudy focuses on deferred defecation. A third study assessed defecatory parameters as a function of the stiffness of Fecobionics. Pelvic floor function will also be assessed through vaginal measurements as well as Fecobionics may be endoscopically placed in sigmoid colon. Finally, a substudy assessed intestinal parameters after insertion of Fecobionics through a stoma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Incontinence, Constipation

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Fecobionics studies
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Fecobionics
Intervention Description
Fecobionics is a new device for studying defecation
Primary Outcome Measure Information:
Title
Decreased anorectal pressure assessed with the Fecobionics device
Description
The number of participants with low anorectal pressure during defecation
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Decreased anorectal mechanical stress assessed with the Fecobionics device
Description
The number of participants with low anorectal mechanical stress during defecation
Time Frame
1 year
Title
Decreased anorectal angle assessed with the Fecobionics device
Description
The number of participants with small anorectal angle during defecation
Time Frame
1 year
Title
Wave-like decrease in cross-sectional area with the Fecobionics device
Description
The amount of recordings with retrograde intestinal ripples
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy subjects: Asymptomatic healthy persons aged over 18 years who can give informed consent. CC (Chronic Constipation) Patients: Patients over 18 with history of FI for over 3months, who are able to give consent. FI (Fecal Incontinence) patients: Patients over 18 with history of FI for over 3months, who are able to give consent. Patients with a stoma who are over 18 years and able to give consent. Exclusion Criteria: Healthy subjects: Persons with a history of constipation or fecal incontinence, prior abdominal surgery, medication, and diseases, especially chronic diseases that affect bowel function and defecation. Pregnant women will also be excluded. CC Patients: Patients, who are not willing to undergo the proposed test program and patients with prior anorectal or intestinal surgery. Pregnant women and patients with chronic dehydration and on medications like opioids will also be excluded. FI patients: 1) Patients who are not willing to undergo the specified tests in this study, 2) Pregnant women and 3) Patients who has had anorectal surgery or bowel resection. Patients with stoma: Patients, who are not willing to undergo the proposed test program and patients who have inflammation or symptoms related to the stoma.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kaori Futaba
Phone
0085235051495
Email
kfutaba@surgery.cuhk.edu.hk
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong
ZIP/Postal Code
000000
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wing Wa Leung, PhD
Phone
008525052951
Email
leungww@surgery.cuhk.edu.hk
Facility Name
Department of Surgery, Prince of Wales Hospital
City
Hong Kong
ZIP/Postal Code
0000
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kaori Futaba
Phone
0085235051495
Email
kfutaba@surgery.cuhk.edu.hk

12. IPD Sharing Statement

Citations:
PubMed Identifier
35363631
Citation
Futaba K, Chen SC, Leung WW, Wong C, Mak T, Ng S, Gregersen H. Fecobionics Evaluation of Biofeedback Therapy in Patients With Fecal Incontinence. Clin Transl Gastroenterol. 2022 May 1;13(5):e00491. doi: 10.14309/ctg.0000000000000491.
Results Reference
derived
PubMed Identifier
33949343
Citation
Gregersen H, Chen SC, Leung WW, Wong C, Mak T, Ng S, Daming S, Futaba K. Characterization of Patients With Obstructed Defecation and Slow Transit Constipation With a Simulated Stool. Clin Transl Gastroenterol. 2021 May 5;12(5):e00354. doi: 10.14309/ctg.0000000000000354.
Results Reference
derived
PubMed Identifier
33779850
Citation
Chen SC, Futaba K, Leung WW, Wong C, Mak T, Ng S, Gregersen H. Fecobionics assessment of the effect of position on defecatory efficacy in normal subjects. Tech Coloproctol. 2021 May;25(5):559-568. doi: 10.1007/s10151-021-02439-2. Epub 2021 Mar 29.
Results Reference
derived
PubMed Identifier
31800543
Citation
Gregersen H, Chen SC, Leung WW, Wong C, Mak T, Ng S, Futaba K. Novel Fecobionics Defecatory Function Testing. Clin Transl Gastroenterol. 2019 Dec;10(12):e00108. doi: 10.14309/ctg.0000000000000108.
Results Reference
derived

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Studies in Patients With Defecatory Disorders

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