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Acute diarrhea continues to be a major cause of childhood morbidity and mortality in developed and developing countries. Prevention and treatment of dehydration are the mainstays of therapy. Rehydration can be achieved with oral rehydratation solution (ORS). Even though ORS has reduced the mortality and morbidity very significantly, it has no effect on the duration of diarrhea, stool consistency and frequency and remains underused. ESPGHAN and ESPID published together an evidence based guideline and stated that in the management of acute gastroenteritis rehydration is the key treatment and that selected probiotics may reduce the duration and intensity of symptoms and can be used as an adjuvant to ORS. A recent Cochrane review including 56 trials in children concluded that specific probiotics reduce the duration of diarrhea with about 24 hours and decrease the frequency of defecation on the second day. Current evidence also indicates that probiotic effects are strain-specific. Lactobacillus LGG and Saccharomyces boulardii are the best studied strains. However, more research is needed to guide the use of particular probiotic regimens and strains and as there is still no evidence of efficacy for many preparations. The aim of this study was to evaluate effects of different probiotics on the duration of acute infectious diarrhea.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Probiotic | Active Comparator | Saccharomyces boulardii 1 x 250 mg per day for 5 days, PO or Lactobacillus GG 1 x 10(9) CFU per day for 5 days or Lactobacillus reuteri 1 x 10(8) CFU per day for 5 days |
|
| Control | Active Comparator | ORS-ad libitum |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Probiotic | Dietary Supplement | Comparison of probiotics vs. ORS |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Duration of diarrhea | Duration of diarrhea, since the beginning of the intervention, evaluated with Bristol scoring scale | Day 7 |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of children with diarrhea at the 3rd day of intervention | Percentage of children with diarrhea at the 3rd day of intervention | Day 3 |
| Duration of hospitalization | Lenght of stay of hoospitalization |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Ener C Dinleyici, MD | Eskisehir Osmangazi University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Dr. Sami Ulus Research and Training Hospital of Women's and Children's Health and Diseases | Ankara | Turkey (Türkiye) | ||||
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| ID | Term |
|---|---|
| D003967 | Diarrhea |
| ID | Term |
|---|---|
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D019936 | Probiotics |
| C034130 | ORALIT |
| ID | Term |
|---|---|
| D019587 | Dietary Supplements |
| D005502 | Food |
| D000066888 | Diet, Food, and Nutrition |
| D010829 | Physiological Phenomena |
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| ORS |
| Dietary Supplement |
ORS ad libitum |
|
| Day 5 |
| Safety of probiotics | All clinical conditions (related with probiotics) should be noted. | 5 days of intervention |
| Sisli Etfal Training and Research Hospital, |
| Istanbul |
| 34000 |
| Turkey (Türkiye) |
| Umraniye Education & Research Hospital, Department of Pediatrics | Istanbul | Turkey (Türkiye) |
| D019602 |
| Food and Beverages |