Functional Constipation Clinical Trial
Official title:
Randomized, Placebo-controlled Double-blind Cross-over Study to Evaluate the Effects of Short-chain Fructooligosaccharides on Stool Frequency in Constipated Subjects
Rationale: The dietary short-chain fructooligosaccharides have been shown to increase fecal
bacterial mass and fermentation metabolites which might stimulate gut motility. Therefore,
these dietary non-digestible carbohydrates might relieve functional constipation.
Objective: Study the effect of short-chain fructooligosaccharides on functional
constipation.
Study design: A 16-week, randomized, placebo-controlled, double-blind cross-over trial with
intervention periods of 4 weeks with a run-in period of 4 weeks and a wash-out period of 4
weeks.
Study population: Human subjects with functional constipation according to ROMEIII criteria
(total n=120; male and female; 18-75 yr).
Intervention: Placebo and one out of 3 dosages of short-chain fructo-oligosaccharides,
(Degree of Polymerisation of 3-5; 2, 4 and 8 g/day) for 4 weeks. scFOS will be given as oral
chews.
Main study parameters: The primary parameter is the number of complete bowel movements per
day in subjects with functional constipation according to Rome III criteria. Secondary
outcomes are Stool consistency (Bristol Stool Scale), Stool frequency, Severity of symptoms
(Constipation Scoring System; CSS) and Quality of Life (Patient Assessment of Constipation
Quality of Life; PAC-QoL).
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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