Soy Polysaccharide Fiber for the Treatment of Chronic Constipation in Children: a Randomized, Double-blind Trial (SOYFIBER)
Primary Purpose
Constipation
Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Soy polysaccharide fiber
Sponsored by
About this trial
This is an interventional treatment trial for Constipation focused on measuring clinical trial, dietary fiber, constipation, children
Eligibility Criteria
Inclusion Criteria:
- Patients over two years of age at first consultation and chronic functional constipation were included. Chronic constipation was defined by the occurrence of any of the following, for at least 2 weeks, independently of stool frequency: passage of hard, scybalous, pebble-like or cylindrical cracked stools, straining or painful defecation, passage of large stools that may clog the toilet, or stool frequency less than 3 per week.
Exclusion Criteria:
- The exclusion criteria applied were organic constipation, regular use of dietary fiber in the preceding 30 days or drugs causing constipation.
Sites / Locations
- Division of Pediatric Gastroenterology UNIFESP
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Soy polysaccharide fiber
purified soy extract, with no fiber)
Arm Description
Dietary fiber for treatment of chronic constipation in children
blinded control group
Outcomes
Primary Outcome Measures
Clinical response
Frequency of stool passage, paiful defecation, stool consistency
Secondary Outcome Measures
total and segmental colonic transit time and fecal weight and moisture
Colonic transit time was evaluated by the technique of Metcalf et al. In brief, a plain abdominal radiograph performed after 24 hours from the last ingestion of 3 sets of 20 distinctive radio-opaque markers taken on 3 consecutive days. In the presence of > 20% of the markers, a further radiography was taken on the 7th day. The colonic segments were delimitated according to Arhan et al. The patients were instructed to collect the 3-day stools separately from the urine. The collected stools were used to determine the fecal weight and moisture.
Full Information
NCT ID
NCT01267370
First Posted
December 27, 2010
Last Updated
December 27, 2010
Sponsor
Federal University of São Paulo
Collaborators
Maria Eugênia Farias Almeida Motta, Soraia Tahan, Mauro Batista de Morais
1. Study Identification
Unique Protocol Identification Number
NCT01267370
Brief Title
Soy Polysaccharide Fiber for the Treatment of Chronic Constipation in Children: a Randomized, Double-blind Trial
Acronym
SOYFIBER
Official Title
Soy Polysaccharide Fiber for the Treatment of Chronic Constipation in Children: a Randomized, Double-blind Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2003
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
December 2002 (Actual)
Study Completion Date
October 2003 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Federal University of São Paulo
Collaborators
Maria Eugênia Farias Almeida Motta, Soraia Tahan, Mauro Batista de Morais
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study tested the hypothesis that soy polysaccharide fiber reduces clinical symptoms of chronic constipation.
Detailed Description
The study was performed out at outpatient clinic of Pediatric Gastroenterology at the Federal University of São Paulo (São Paulo, Brazil), located in the southeastern region of Brazil. It is a public referral hospital for pediatric gastroenterology attendance in the Metropolitan area of the São Paulo and in Brazil. In general, the patients go to consultation after a referral from a primary care center.
Study design and sample size The design was a randomized double-blind trial, placebo-controlled study. Sample size was calculated by the formula of comparison of two proportions, using clinical improvement as a primary outcome. It had been previously calculated that a minimum of 14 patients in each group will give a power of 80% to detect a effect size of 50% with significance at the level of 5% (one-sided).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation
Keywords
clinical trial, dietary fiber, constipation, children
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Soy polysaccharide fiber
Arm Type
Active Comparator
Arm Description
Dietary fiber for treatment of chronic constipation in children
Arm Title
purified soy extract, with no fiber)
Arm Type
Placebo Comparator
Arm Description
blinded control group
Intervention Type
Dietary Supplement
Intervention Name(s)
Soy polysaccharide fiber
Other Intervention Name(s)
Soy polysaccharide fiber (Pró-fibra®), Purified soy extract, with no fiber (Soyac®)
Intervention Description
Dietary Supplement: Soy polysaccharide fiber First, disimpaction was carried out with phosphate enemas for 1 to 3 days. After the children have been "cleaned out", they received a soy polysaccharide fiber supplement (powder containing 70 g of fiber/100 g) or placebo (purified soy extract, with no fiber) for 6 weeks. Fiber and placebo were given as a standard dose for the different age groups (median of 0,57 g/kg/day) - 2 to 5 years, 10 g/day; 6 to 9 years, 15 g/day; and > 10 years, 20 g/day.
The child that had fecal impaction (a dilated rectum filled with a large amount of stool on rectal examination) during the follow-up was treated by administering phosphate enemas for 1 to 3 consecutive days.
Arms: Soy polysaccharide fiber, purified soy extract, with no fiber
Other Names:
Soy polysaccharide fiber (Pró-fibra®) Purified soy extract, with no fiber (Soyac®)
Primary Outcome Measure Information:
Title
Clinical response
Description
Frequency of stool passage, paiful defecation, stool consistency
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
total and segmental colonic transit time and fecal weight and moisture
Description
Colonic transit time was evaluated by the technique of Metcalf et al. In brief, a plain abdominal radiograph performed after 24 hours from the last ingestion of 3 sets of 20 distinctive radio-opaque markers taken on 3 consecutive days. In the presence of > 20% of the markers, a further radiography was taken on the 7th day. The colonic segments were delimitated according to Arhan et al. The patients were instructed to collect the 3-day stools separately from the urine. The collected stools were used to determine the fecal weight and moisture.
Time Frame
6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients over two years of age at first consultation and chronic functional constipation were included. Chronic constipation was defined by the occurrence of any of the following, for at least 2 weeks, independently of stool frequency: passage of hard, scybalous, pebble-like or cylindrical cracked stools, straining or painful defecation, passage of large stools that may clog the toilet, or stool frequency less than 3 per week.
Exclusion Criteria:
The exclusion criteria applied were organic constipation, regular use of dietary fiber in the preceding 30 days or drugs causing constipation.
Facility Information:
Facility Name
Division of Pediatric Gastroenterology UNIFESP
City
São Paulo
ZIP/Postal Code
04039-031
Country
Brazil
12. IPD Sharing Statement
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Soy Polysaccharide Fiber for the Treatment of Chronic Constipation in Children: a Randomized, Double-blind Trial
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