Investigation of Supra Fiber in the Treatment of Adults With Constipation
Primary Purpose
Constipation
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Supra Fiber
Psyllium
Sponsored by
About this trial
This is an interventional treatment trial for Constipation
Eligibility Criteria
Inclusion Criteria:
- Constipation as defined by Rome III criteria (3,4). Also, patients should have insufficient criteria for IBS, and only rarely experience loose stools without the use of laxatives.
- Adults between the ages of 18-75 years
Exclusion Criteria:
- Patients taking drugs that are known to be constipating will be excluded or asked to discontinue medications for at least 2 weeks and reassessed. Patients who remain constipated will be eligible for enrollment.
- Co-morbid illnesses such as severe cardiovascular disease, chronic renal failure
- Previous gastrointestinal surgery except cholecystectomy and appendectomy.
- Neurologic diseases such as multiple sclerosis, strokes, spinal cord injuries, and those who have problems with cognizance, i.e. a mini-mental score of <15 and/or are legally blind
- Hirschsprung' s disease, or active local anorectal problems such as anal fissures, bleeding hemorrhoids,
- Alternating constipation and diarrhea and those who fulfill the Rome-III criteria for irritable bowel syndrome.
- Subjects with a known allergy to psyllium or plums.
Sites / Locations
- University of Iowa Hospitals and Clinics
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Supra Fiber
Psyllium
Arm Description
Outcomes
Primary Outcome Measures
Number of Complete Spontaneous Bowel Movements (CSBM) per week
1. Number of Complete Spontaneous Bowel Movements (CSBM) per week. This will be analyzed from the daily stool diaries (Appendix 1). The CSBM provides a more robust and better assessment of the overall change in bowel function that takes into account not only the stool frequency but also the completeness and satisfaction with bowel function. A CSBM is defined as a bowel movement that is produced without the use of additional laxatives, suppositories or enemas in the previous 24 hours, other than the study medication.
Secondary Outcome Measures
Global Relief of Constipation
Global relief of constipation.
Other Parameters of bowel function including stool frequency, stool consistency (Bristol Stool Scale), Straining effort, Feeling of complete evacuation, bloating, and distension
Full Information
NCT ID
NCT01288508
First Posted
January 19, 2011
Last Updated
September 16, 2014
Sponsor
Augusta University
1. Study Identification
Unique Protocol Identification Number
NCT01288508
Brief Title
Investigation of Supra Fiber in the Treatment of Adults With Constipation
Official Title
Investigation of Supra Fiber in the Treatment of Adults With Constipation-A Double-blind Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2014
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
September 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Augusta University
4. Oversight
5. Study Description
Brief Summary
Background: Whether Supra-Fiber, a plum-derived fiber supplement is useful in the treatment of constipation is not known. Supra Fiber is the first fiber supplement that has a blend of whole food fruit as its main ingredient. It contains prunes, pomegranates, blueberries, and Acai berries. Unlike psyllium, which is mostly (90%) insoluble fiber, Supra Fiber is a balanced (50%) blend of insoluble and soluble fiber. This may provide the beneficial effects of fiber, and eliminate potential adverse symptoms of fiber such as bloating, distention, hard bulky stools and excess gas. In this study, we expect to not only evaluate the efficacy but also the palatability and tolerability of Supra Fiber in the treatment of chronic constipation.
Aims:
To investigate and compare the effects of Supra Fiber (5 grams BID) or psyllium (5 grams BID) on the number of complete spontaneous bowel movements per week, and bowel symptoms.
To examine the effects of fiber supplements on taste and quality of life in adults with functional chronic constipation in a randomized, double-blind, parallel group controlled trial.
Methods: We propose to enroll 90 subjects with functional constipation in a single blinded, randomized, cross-over study comparing 4 weeks of Supra Fiber with 4 weeks of treatment with Psyllium
Data analysis: The primary outcome measure will be the global relief of constipation symptoms as rated by the subject at the end of each phase of the study. Additionally, we will assess several secondary outcome measures that will include the number of Complete Spontaneous Bowel Movements (CSBM) per week, Quality of Life , psychological profile, patient rating of taste on a VAS scale, patient rating of bloating, distension, satiety and fullness and patient rating of constipation-related symptoms.
Expected results: We anticipate that treatment with Supra Fiber will improve symptoms of constipation compared to the baseline. This improvement will be comparable or superior to that achieved with psyllium treatment. Additionally, Supra Fiber will offer a natural, food based, convenient and more tasty alternative to over-the-counter laxatives and fiber supplements.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
89 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Supra Fiber
Arm Type
Active Comparator
Arm Title
Psyllium
Arm Type
Active Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Supra Fiber
Intervention Description
2 tablespoons of fiber taken with 8oz water taken twice a day for 30 days
Intervention Type
Dietary Supplement
Intervention Name(s)
Psyllium
Intervention Description
1 tablespoon of fiber taken with 8 oz water twice a day for 30 days
Primary Outcome Measure Information:
Title
Number of Complete Spontaneous Bowel Movements (CSBM) per week
Description
1. Number of Complete Spontaneous Bowel Movements (CSBM) per week. This will be analyzed from the daily stool diaries (Appendix 1). The CSBM provides a more robust and better assessment of the overall change in bowel function that takes into account not only the stool frequency but also the completeness and satisfaction with bowel function. A CSBM is defined as a bowel movement that is produced without the use of additional laxatives, suppositories or enemas in the previous 24 hours, other than the study medication.
Time Frame
9 Weeks
Secondary Outcome Measure Information:
Title
Global Relief of Constipation
Description
Global relief of constipation.
Other Parameters of bowel function including stool frequency, stool consistency (Bristol Stool Scale), Straining effort, Feeling of complete evacuation, bloating, and distension
Time Frame
9 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Constipation as defined by Rome III criteria (3,4). Also, patients should have insufficient criteria for IBS, and only rarely experience loose stools without the use of laxatives.
Adults between the ages of 18-75 years
Exclusion Criteria:
Patients taking drugs that are known to be constipating will be excluded or asked to discontinue medications for at least 2 weeks and reassessed. Patients who remain constipated will be eligible for enrollment.
Co-morbid illnesses such as severe cardiovascular disease, chronic renal failure
Previous gastrointestinal surgery except cholecystectomy and appendectomy.
Neurologic diseases such as multiple sclerosis, strokes, spinal cord injuries, and those who have problems with cognizance, i.e. a mini-mental score of <15 and/or are legally blind
Hirschsprung' s disease, or active local anorectal problems such as anal fissures, bleeding hemorrhoids,
Alternating constipation and diarrhea and those who fulfill the Rome-III criteria for irritable bowel syndrome.
Subjects with a known allergy to psyllium or plums.
Facility Information:
Facility Name
University of Iowa Hospitals and Clinics
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52246
Country
United States
12. IPD Sharing Statement
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Investigation of Supra Fiber in the Treatment of Adults With Constipation
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