Diarrhea Clinical Trial
Official title:
Research of Change of Microbial System Intestines and Efficacy for Probiotic Treatment of Persistent Diarrhea in Children
Verified date | May 2024 |
Source | National Children's Hospital, Vietnam |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Persistent diarrhea is a common health problem worldwide, particularly in low-income countries. Approximately 3% to 20% of acute diarrhea episodes in children under 5 years of age become persistent diarrhea. Persistent diarrhea causes malnutrition, weight loss, and dehydration, as well as increasing treatment costs and the risk of mortality. One of the main causes of persistent diarrhea is the overgrowth and spread of bacteria, as well as viral infections that can disrupt the balance of microorganisms in the gut. Antibiotics are effective in treating bacterial infections that cause persistent diarrhea in children, but not against viral or parasitic infections. Overuse of antibiotics can lead to the growth of antibiotic-resistant bacteria, which poses a significant public health concern. Probiotics play a vital role in maintaining a healthy balance. Bacillus probiotic strains have an advantage over Lactobacillus probiotics as they can form spores that resist environmental stressors like heat, acid, and bile. This makes them more likely to survive the harsh conditions of the digestive tract and provide health benefits by reaching the intestines intact. Here, the investigators propose high-dose Bacillus spore probiotic supplementation as a potential solution for treating patients with persistent diarrhea. The aim of the study is to assess the efficacy of two types of Bacillus probiotics which conclude LiveSpo CLAUSY (2 billion B. clausii) and LiveSpo DIA 30 (5 billion B. subtilis, B. clausii and B. coagulans) in supporting the treatment of children with persistent diarrhea. Study Population: sample size is 150 patients and 30 healthy children. The study is carried out at Vietnam National Children's Hospital. Description of Study Intervention: Totally 150 eligible patients are divided randomly into 3 groups (n = 50/group each): Patients in the Control group received the routine treatment and 2-3 times/day RO water while the patients in the probiotics group received 2-3 times/day LiveSpo DIA 30 or LiveSpo CLAUSY in addition to the same standard of care treatment. The standard treatment regimen is 5-9 days but can be extended further depending on the severity of the patient. Healthy children are grouped into the "Healthy" group solely for the purpose of comparing the microbiota between healthy children with those patients before and after treatment. Therefore, the Healthy group does not receive any intervention. Study duration: 18 months
Status | Active, not recruiting |
Enrollment | 165 |
Est. completion date | June 15, 2024 |
Est. primary completion date | December 25, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 2 Months to 24 Months |
Eligibility | Inclusion Criteria: - Patients who are between 2 months and 24 months old - Have loose or unusual watery stools more than 3 times per day, lasting between 14 and 30 days - Parents of the pediatric patient agree to participate in the study, explain and sign the research consent form Exclusion Criteria: - The patient had any systemic illness other than diarrhea on admission. - Patient has any systemic complications during treatment. |
Country | Name | City | State |
---|---|---|---|
Vietnam | Department of Gastroenterology, Vietnam National Children's Hospital | Hanoi |
Lead Sponsor | Collaborator |
---|---|
National Children's Hospital, Vietnam |
Vietnam,
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* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in days of treatment for typical symptoms of persistent diarrhea | Changes in days of treatment for typical symptoms of persistent diarrhea, including:
the frequency of bowel movements per day (times/day) the presence of mucus in stool (2 - lots of mucus, 1 - less mucus, 0 - no mucus) the Bristol Stool Score ( 1 - Type 1, 2 - Type 2, 3 - Type 3, 4 - Type 4, 5 - Type 5A, 6 - Type 5B) |
Day 0 to Day 12 | |
Secondary | Changes in presence of white blood cells and red blood cells by stool microscopy | Changes in presence of white blood cells (yes/no) and red blood cells (yes/no). | Day 3 and Day 5 compared to Day 0 | |
Secondary | Changes in Intestinal microbiota | Changes in intestinal microbiota (bacterial species composition) in the stool samples of patients with persistent diarrhea before (Day 0) and after treatment (Day 3 or/and 7), as well as with that of healthy children (Day 0, no intervention) | Day 3 or/and Day 7 compared to Day 0 | |
Secondary | Changes in cytokines levels of blood samples | Changes in levels (pg/mL) in several cytokines, including tumor necrosis factor-a (TNF-a), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), interleukin-17 (IL-17), interleukin-23 (IL-23) | Day 5 compared to Day 0 | |
Secondary | Changes in IgA levels in both stool and blood samples | Changes in levels (µg/mL) of pro-inflammatory IgA in both stool and blood samples | Day 5 compared to Day 0 | |
Secondary | Change the stool pH values | Change the pH values of stool samples at day 3-5 (after treatment) compared with day 0 (before treatment) | Day 3 and Day 5 compared to Day 0 |
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