Optimizing the Management of Acute Diarrhoeal Disease
Acute Gastroenteritis
About this trial
This is an interventional treatment trial for Acute Gastroenteritis focused on measuring diarrhoea, gastroenteritis, rapid diagnostics, probiotics
Eligibility Criteria
Inclusion Criteria:
- acute diarrhoeal illness (>= 3 stools in 24 hour period)
Exclusion Criteria:
- diarrhoeal illness >=14 days
- bloody stool
- known inflammatory bowel disease, cystic fibrosis, or malignancy
- live in a household with someone else documented to have a bacterial or parasitic enteric infection of defined aetiology
- live outside catchment areas
- no permanent address
- no access to mobile phone
- previous participation in this study
- nosocomial diarrhoea
Sites / Locations
- Princess Marina Hospital
- Deborah Retief Hospital
- Scottish Livingstone Hospital
- Bamalete Lutheran Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Other
Other
Placebo Comparator
Rapid diagnostics and probiotic
Rapid diagnostics and placebo
No rapid diagnostics and probiotic
No rapid diagnostics and placebo
Participants randomized to this arm will have rapid enteric diagnostics performed on the day of enrolment. Those found to have a treatable pathogen will be prescribed antimicrobials that day. Participants will also be given Lactobacillus reuteri DSM 17938 5 x 10e8 cfu/mL x 60 days.
Participants randomized to this arm will have rapid enteric diagnostics performed on the day of enrolment. Those found to have a treatable pathogen will be prescribed antimicrobials that day. Participants will also be given placebo x 60 days.
Participants randomized to this arm will have stool specimens processed after the conclusion of the study. Participants will also be given Lactobacillus reuteri DSM 17938 5 x 10e8 cfu/mL x 60 days.
Participants randomized to this arm will have stool specimens processed after the conclusion of the study. Participants will also be given placebo x 60 days.