HyGIeaCare Procedure for Chronic Constipation
Primary Purpose
Constipation - Functional
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
colon irrigation
Sponsored by
About this trial
This is an interventional treatment trial for Constipation - Functional
Eligibility Criteria
Inclusion Criteria:
- Patient has chronic constipation according to Rome III criteria
- Patient has not experienced relief of symptoms following treatment with available therapies (osmotic and stimulant laxatives) for at least one month at recommended doses.
Exclusion Criteria:
- Patient has functional bowel disorders characterized by alternating bowel habits (diarrhea/constipation)
- Patient has secondary constipation (colonic obstruction, medications, metabolic cause)
- Patient has any other condition that, in the opinion of the investigator, may adversely affect the compliance or safety of the patient or would limit the patient's ability to complete the study.
Patient has any of the contraindications listed below:
- Cardiac: Congestive heart failure (NYHA class III or IV or EF <50%)
- GI: Intestinal perforation, carcinoma of the rectum, fissures or fistula, severe hemorrhoids, abdominal hernia, recent colon or rectal surgery, or abdominal surgery
- GU: Renal insufficiency (CC < 60 ml/min/173m2), cirrhosis with ascites
- Abdominal surgery within the last 6 months
- Pregnancy
Sites / Locations
- Mayo Clinic
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
pre colon irrigation diaries followed by post diaries
Arm Description
4 week bowel movement and rescue medication diaries will be compared to same diaries used 4 weeks after the colon irrigation procedure
Outcomes
Primary Outcome Measures
Change in number of BMs
Change in the number of bowel movements per week from the baseline period (4 weeks) to the four weeks of the post-HyGIeaCare period.
Secondary Outcome Measures
Change in constipation score and discomfort score (GISSI)
Gastrointestinal Symptom Severity Index (GISSI) constipation/difficult defecation cluster and abdominal pain/discomfort cluster
Change in rescue medications used
Review of the number of times rescue medications are used for constipation relief
Full Information
NCT ID
NCT03335969
First Posted
October 30, 2017
Last Updated
September 20, 2019
Sponsor
HyGIeaCare, Inc.
Collaborators
Biostatistical Consulting, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT03335969
Brief Title
HyGIeaCare Procedure for Chronic Constipation
Official Title
Evaluation of the HyGIeaCare Procedure for Patients With Chronic Constipation
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Withdrawn
Why Stopped
no patients recruited
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
March 1, 2019 (Actual)
Study Completion Date
March 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
HyGIeaCare, Inc.
Collaborators
Biostatistical Consulting, Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To assess the safety and clinical effectiveness of using the FDA cleared HyGIeaCare System to relieve constipation in patients not responding to standard laxative treatment. Each patient will serve as their own control by comparing their bowel habits in a diary 4 weeks prior to colon irrigation to the bowel habits in their diary 4 weeks post colon irrigation.
Detailed Description
This study has a single center, prospective, open label design. Patients will serve as their own control.
The population will include patients with chronic constipation according to Rome III criteria who failed to improve with currently available therapy (osmotic and stimulant laxatives, used for at least one month at recommended dose).
Once patients are consented to participate in the study, they will complete the Gastrointestinal Symptom Severity Index (GISSI) questionnaire. Patients will complete the 4 Week Bowel Movement Diary and 4 Week Medication Use Diary for the 4-weeks prior to their HyGIeaCare procedure. The Medication Use Diary will include any rescue medications taken above and beyond what patients are taking as part of their constipation regimen.
The patient will schedule their HyGIeaCare procedure directly with the HyGIeaCare Clinic. The nurse manager can be reached at 480-750-2333. The clinic is located at 4001 E. Baseline Road, Gilbert, AZ. The nurse manager will provide the patient with any instructions needed prior to their HyGIeaCare procedure. HyGIeaCare will furnish the principle investigator with the complete patient care records after the irrigation procedure has been completed.
Following the 4 weeks post the patient's HyGIeaCare procedure, the patient will complete a new 4 Week Bowel Movement Diary and 4 Week Medication Use Diary for the 4-weeks post their HyGIeaCare procedure. The patient will bring these documents to their clinic follow-up visit. At this visit the patient will complete another GISSI questionnaire and will be evaluated for possible adverse events.
Patient data will be collected on hard copy case report forms (CRFs) and then entered into an electronic database.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation - Functional
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Each patient will serve as their own control by comparing their bowel habits in a diary 4 weeks prior to colon irrigation to the bowel habits in their diary 4 weeks post colon irrigation.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
pre colon irrigation diaries followed by post diaries
Arm Type
Experimental
Arm Description
4 week bowel movement and rescue medication diaries will be compared to same diaries used 4 weeks after the colon irrigation procedure
Intervention Type
Device
Intervention Name(s)
colon irrigation
Other Intervention Name(s)
HyGIeaCare System
Intervention Description
Study is to compare bowel movement patterns before and after colon irrigation.
Primary Outcome Measure Information:
Title
Change in number of BMs
Description
Change in the number of bowel movements per week from the baseline period (4 weeks) to the four weeks of the post-HyGIeaCare period.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Change in constipation score and discomfort score (GISSI)
Description
Gastrointestinal Symptom Severity Index (GISSI) constipation/difficult defecation cluster and abdominal pain/discomfort cluster
Time Frame
8 weeks
Title
Change in rescue medications used
Description
Review of the number of times rescue medications are used for constipation relief
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient has chronic constipation according to Rome III criteria
Patient has not experienced relief of symptoms following treatment with available therapies (osmotic and stimulant laxatives) for at least one month at recommended doses.
Exclusion Criteria:
Patient has functional bowel disorders characterized by alternating bowel habits (diarrhea/constipation)
Patient has secondary constipation (colonic obstruction, medications, metabolic cause)
Patient has any other condition that, in the opinion of the investigator, may adversely affect the compliance or safety of the patient or would limit the patient's ability to complete the study.
Patient has any of the contraindications listed below:
Cardiac: Congestive heart failure (NYHA class III or IV or EF <50%)
GI: Intestinal perforation, carcinoma of the rectum, fissures or fistula, severe hemorrhoids, abdominal hernia, recent colon or rectal surgery, or abdominal surgery
GU: Renal insufficiency (CC < 60 ml/min/173m2), cirrhosis with ascites
Abdominal surgery within the last 6 months
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah Umar, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
25842355
Citation
Crowell MD, Umar SB, Lacy BE, Jones MP, DiBaise JK, Talley NJ. Multi-Dimensional Gastrointestinal Symptom Severity Index: Validation of a Brief GI Symptom Assessment Tool. Dig Dis Sci. 2015 Aug;60(8):2270-9. doi: 10.1007/s10620-015-3647-3. Epub 2015 Apr 5.
Results Reference
background
PubMed Identifier
25803399
Citation
Sommers T, Corban C, Sengupta N, Jones M, Cheng V, Bollom A, Nurko S, Kelley J, Lembo A. Emergency department burden of constipation in the United States from 2006 to 2011. Am J Gastroenterol. 2015 Apr;110(4):572-9. doi: 10.1038/ajg.2015.64. Epub 2015 Mar 24.
Results Reference
result
Links:
URL
http://www.alliedacademies.org/articles/randomized-trial-comparing-high-volume-rectal-water-irrigation-with-standard-4-l-splitdose-peg-preparation-before-colonoscopy.pdf
Description
Randomized Trial Comparing High Volume Rectal Water Irrigation with Standard 4 L Split-Dose PEG Preparatoin before Colonoscopy
URL
https://www.omicsonline.org/open-access/hygieacare-preparation-for-colonoscopya-technical-update-for-success-2161-069X-1000458.php?aid=79003
Description
HyGIeaCare Preparation for Colonoscopy-A Technical Update for Success
URL
https://www.google.com/search?q=Use+of+health+care+resources+and+cost+of+care+for+adults+with+constipation.+Clin+Gastroenterol+Hepatol.&rlz=1C1CHBF_enUS700US700&oq=Use+of+health+care+resources+and+cost+of+care+for+adults+with+constipation.+Clin+Gastroenterol+Hepatol.&aqs=chrome..69i57.814j0j4&sourceid=chrome&ie=UTF-8
Description
Use of health care resources and cost of care for adults with constipation
Learn more about this trial
HyGIeaCare Procedure for Chronic Constipation
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