Constipation Clinical Trial
Official title:
Mixed Natural Prebiotic-Fibers Impact on Stool Frequency and Fecal Microbiota in Constipated Thai Adults: A Randomized Clinical Trial.
Verified date | February 2024 |
Source | Mahidol University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Mixed Natural Prebiotic-Fibers Impact on Stool Frequency and Fecal Microbiota in Constipated Thai Adults: A Randomized Clinical Trial.
Status | Active, not recruiting |
Enrollment | 98 |
Est. completion date | April 19, 2024 |
Est. primary completion date | July 22, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility | Inclusion Criteria: - Healthy adults with a Body mass index (BMI) of 16.00 to 29.99 kg/m2 - Self-reported constipation according to the Rome IV criteria Exclusion Criteria: - Pregnancy - Crohn's disease or any other inflammatory bowel disease - Pelvic floor dyssynergia - Have congenital diseases such as liver disease, diabetes, and thyroid dysfunction. hypercalcemia neurological disease - Drink alcohol or smoke regularly. - During the past 1 month or while in the project, have received antibiotics, steroids, NSAIDs, blood pressure-lowering drugs, antidepressants, anticonvulsants, or Parkinson's disease medications - History of food allergy to Haruna's ingredients - There has been a change in body weight (increase or decrease of 5 kilograms over a period of 6 months). - During the past 2 weeks or while in the project, have received probiotics or other prebiotics |
Country | Name | City | State |
---|---|---|---|
Thailand | Mahidol University | Nakhon Pathom |
Lead Sponsor | Collaborator |
---|---|
Mahidol University |
Thailand,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Stool Frequency | Stool frequency during the intervention period was determined by modified Constipation scoring system using questionnaire with the following variables: frequency of bowel movements; painful evacuation effort; feeling of incomplete evacuation; abdominal pain; minutes in lavatory per attempt; type of assistance; unsuccessful attempts for evacuation. This consists of six items that are scored using a five-point Likert scale that ranges from 0 (none of the time) to 4 (all of the time) and one item that is rated on a 0-2 scale. A total score can range from 0 (normal) to 26 (severe constipation). | 12 weeks | |
Primary | Change in Fecal Microbiota | Change in Bifidobacterium relative abundance with 2log ratio of relative abundance, during the intervention period, compared between prebiotic arm and placebo arm. Subjects with an increase in Bifidobacterium relative abundance were considered to have a good response. | 12 weeks | |
Secondary | Change in Stool consistency | Stool consistency during the intervention period was determined by Bristol stool scale score using questionnaire with the following scale score: 1, separate hard lumps, like nuts; 2, sausage-shaped but lumpy; 3, like a sausage but with cracks on its surface; 4, like a sausage or snake, smooth and soft; 5, soft blobs with clear-cut edges; 6, fluffy pieces with ragged edges, a mushy stool; 7, watery, no solid pieces. 1-2 scale indicate constipation. 3-4 scale are ideal stools as they are easier to pass. 5-7 scale may indicate diarrhea and urgency. | 12 weeks |
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