Skip to content

Effects of Pectin Supplementation in Diarrhea-predominant Irritable Bowel Syndrome

Therapeutic Effects of Pectin Supplementation in Patients With Diarrhea-predominant Irritable Bowel Syndrome

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02270268
Enrollment
114
Registered
2014-10-21
Start date
2011-11-30
Completion date
2013-10-31
Last updated
2016-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritable Bowel Syndrome

Keywords

Irritable bowel syndrome, Gut microbiota, Soluble dietary fiber

Brief summary

The purpose of this study is to investigate the effect of pectin, a kind of soluble dietary fiber, on clinical symptoms, gut microbiota and the immune status in patients with diarrhea-predominant irritable bowel syndrome

Detailed description

Patients were randomized to receive either pectin or placebo. Treatment consisted of 6 weeks supplementation with pectin (fiber group) or placebo (maltodextrin). We evaluated the clinical symptoms, gut microbiota and the immune markers in two groups.

Interventions

DIETARY_SUPPLEMENTPectin

Pectin (Andeli Ltd. Yantai, China), 24g/d for six weeks

DIETARY_SUPPLEMENTmaltodextrin

Sponsors

Nanjing PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* All patients(age≧18y) * Admitted for diarrhea-predominant irritable bowel syndrome

Exclusion criteria

* Mental disorders * Cancer * Inflammatory bowel disease

Design outcomes

Primary

MeasureTime frameDescription
efficacy: change of stool frequency, faecal form and clinical symptoms scoresix weeks after inclusionchange from baseline in stool frequency, faecal form (Bristol stool scale) and clinical symptoms score (7-point Likert scale) at six weeks

Secondary

MeasureTime frameDescription
efficacy: gut microbiotasix weeks after inclusionreal-time PCR
efficacy: cytokine ratiossix weeks after inclusionCytokine production

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026