Vomiting in children with acute gastroenteritis is a major factor of failure of oral rehydration therapy. Effective symptomatic treatment of vomiting would lead to an important reduction in the use of Intravenous Fluid Therapy. Available evidence on symptomatic treatment of vomiting shows the efficacy of the most recently registered molecule (ondansetron) but a proper evaluation of antiemetics drugs largely used in clinical practice, such as domperidone, is lacking. The aim of this multicentre, double-blind randomized controlled trial is to compare the efficacy of ondansetron and domperidone for the symptomatic treatment of vomiting in children with acute gastroenteritis who have failed Oral Rehydration Therapy.
Vomiting in children with acute gastroenteritis (AG) is not only a direct cause of fluid loss but it is also a major factor of failure of oral rehydration therapy (ORT). Physicians who provide care to paediatric patients in the emergency department (ED) usually prescribe intravenous fluid therapy (IVT) for mild or moderate dehydration when vomiting is the major symptom. Thus, effective symptomatic treatment of vomiting would lead to an important reduction in the use of IVT and, consequently, of the duration of hospital stay and of frequency of hospital admission. Available evidence on symptomatic treatment of vomiting shows the efficacy of the most recently registered molecule (ondansetron) but a proper evaluation of antiemetics drugs largely used in clinical practice, such as domperidone, is lacking. The aim of this multicentre, double-blind randomized controlled trial conducted in paediatric Emergency Departments is to compare the efficacy of ondansetron and domperidone for the symptomatic treatment of vomiting in children with AG who have failed Oral Rehydration Therapy. The trial results would provide evidence on the efficacy of domperidone, which is largely used in clinical practice despite the lack of proper evaluation and a controversial safety profile, as compared to ondansetron, which is not yet authorized in Italy despite evidence supporting its efficacy in treating vomiting. The trial results would contribute to a reduction in the use of IVT and, consequently, in hospital admissions in children with AG. The design of this RCT, which closely reflect current clinical practice in EDs, will allow immediate transferability of results
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
356
ondansetron syrup (0,15 mg/Kg of body weight)
domperidone syrup (0,5 mg/Kg of body weight)
placebo
Dipartimento di Pediatria, Ospedale Castelli
Verbania, Novara, Italy
Dipartimento di Emergenza Pediatrica, Ospedale Giuseppe Moscati
Avellino, Italy
Dipartimento di Emergenza Pediatrica, P.O. Spedali Civili
Brescia, Italy
Divisione di Emergenza Pediatrica, Ospedale Pediatrico A. Meyer
Florence, Italy
Unità Operativa di Pediatria, Ospedale GB Morgagni
Forlì, Italy
Divisione di Emergenza Pediatrica, Istituto G. Gaslini
Genova, Italy
Dipartimento di Pediatria, Azienda Policlinico di Modena
Modena, Italy
Dipartimento di Emergenza Pediatrica, Azienda Ospedaliera - Università di Padova
Padova, Italy
Dipartimento di Pediatrica, Azienda Ospedaliera- Università di Parma
Parma, Italy
Dipartimento di Pediatrica, Ospedale di Macerata
Province of Macerata, Italy
...and 5 more locations
Percentage of patients needing nasogastric or intravenous rehydration after symptomatic oral treatment failure, defined as vomiting or fluid refusal after the second attempt of ORT.
Time frame: 6 hours
Percentage of subjects needing hospital admission for the same illness;
Time frame: 48 hours
Percentage of subjects needing observation stay for more than 6 hours for the same illness
Time frame: 48 hours
Total emesis duration in the 3 allocation groups;
Time frame: 48 hours
Number of episodes of vomiting in the 3 treatment groups during the follow-up period
Time frame: 48 hours
Percentage of subjects presenting adverse events
Time frame: 48 hours
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