Safety, Efficacy and Cost-effectiveness of Racecadotril in Children With Acute Diarrhea in Mexico (Raceca-Mex)
Diarrhea
About this trial
This is an interventional treatment trial for Diarrhea focused on measuring acute diarrhea, Acute diarrhea (three or more watery or semi-watery bowel movements for at least one day lasting no more than 5 days before being admitted)
Eligibility Criteria
Inclusion Criteria:
- children ≥ 1 month of age and ≤ 24 months of age
- Acute diarrhea (defined as three or more watery or semi-watery bowel movements for at least one day lasting no more than 5 days before being admitted)
- For in hospital group: mild or moderate dehydration
- Signed informed consent letter
Exclusion Criteria:
- previous use of oral antibiotics for more than 48 hours (during the two weeks before the trial
- previous use of anti-diarrheal medication (e.g.: bismuth subsalicylate, adsorbents, Loperamide, combinations)
- chronic pathologies (e.g.: cardiopathies, nephropathies, chronic gastrointestinal pathologies, endocrinopathies)
Sites / Locations
- National Pediatric Institute
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Placebo Comparator
Placebo Comparator
Experimental
ORS-Raceca In hospital Group
ORS-Placebo in hospital group
ORS-Placebo ambulatory group
ORS-Raceca ambulatory group
This group included 135 dehydrated patients which need an oral rehydration therapy in hospital and were assigned to received oral rehydration solution and racecadotril (1.5mg./Kg./t.i.d. doe 5 days) in double blind assigned.
This group included 135 dehydrated patients which need an oral rehydration therapy in hospital and were assigned to received oral rehydration solution and placebo in double blind assigned.
This group included 92 non dehydrated patients which were assigned to received oral rehydration solution and placebo in double blind assigned and ambulatory (in home) bases.
This group included 92 non dehydrated patients which were assigned to received oral rehydration solution and racecadotril (1.5mg./Kg./t.i.d. doe 5 days) in double blind assigned and ambulatory (in home) bases.