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Symptomatic Treatment of Acute Gastroenteritis

Primary Purpose

Gastroenteritis, Vomiting, Acute Gastroenteritis

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Ondansetron
Domperidone
placebo
Sponsored by
IRCCS Burlo Garofolo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroenteritis focused on measuring acute gastroenteritis, vomiting, ondansetron, domperidon, symptomatic treatment

Eligibility Criteria

1 Year - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. age from 1 to 6 years;
  2. presumptive clinical diagnosis of acute gastroenteritis in patients with vomiting, with or without diarrhoea;
  3. more than three episodes of non-bilious, non-bloody vomiting within the previous 24 hours;

Exclusion Criteria:

  1. treatment with antiemetics or antidiarrhoic drugs in the 6 hours prior to access to ED;
  2. underlying chronic diseases (eg, malignancy, gastroesophageal reflux, migraine, renal failure, hypoalbuminemia, liver disease);
  3. severe dehydration: weight loss>10% or standardized clinical dehydration score >=18 for children aged 12-24 months and >=16 for older children;
  4. known hypersensitivity to ondansetron or domperidone;
  5. previous enrolment in the study.

Sites / Locations

  • Dipartimento di Pediatria, Ospedale Castelli
  • Dipartimento di Emergenza Pediatrica, Ospedale Giuseppe Moscati
  • Dipartimento di Emergenza Pediatrica, P.O. Spedali Civili
  • Divisione di Emergenza Pediatrica, Ospedale Pediatrico A. Meyer
  • Unità Operativa di Pediatria, Ospedale GB Morgagni
  • Divisione di Emergenza Pediatrica, Istituto G. Gaslini
  • Dipartimento di Pediatrica, Ospedale di Macerata
  • Dipartimento di Pediatria, Azienda Policlinico di Modena
  • Dipartimento di Emergenza Pediatrica, Azienda Ospedaliera - Università di Padova
  • Dipartimento di Pediatrica, Azienda Ospedaliera- Università di Parma
  • Dipartimento di Emergenza Pediatrica, Ospedale Pediatrico IRCCS Bambino Gesú
  • Dipartimento di Emergenza Pediatrica, Ospedale Infantile Regina Margherita
  • Dipartimento di Pediatria, Ospedale di Treviso
  • Dipartimento di Emergenza Pediatrica, Istituto per la l'Infanzia, IRCCS Burlo Garofolo
  • Unità di Terapia Intensiva Pediatrica, Ospedale Civile Maggiore

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

ondansetron

domperidon

placebo

Arm Description

ondansetron, syrup, 0,15 mg/Kg of body weight, 1 dose

domperidone, syrup, 0,5 mg/Kg of body weight, one dose

placebo, syrup, one dose

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Percentage of subjects needing hospital admission for the same illness;
Percentage of subjects needing observation stay for more than 6 hours for the same illness
Total emesis duration in the 3 allocation groups;
Number of episodes of vomiting in the 3 treatment groups during the follow-up period
Percentage of subjects presenting adverse events

Full Information

First Posted
December 9, 2010
Last Updated
April 17, 2014
Sponsor
IRCCS Burlo Garofolo
Collaborators
Mario Negri Institute for Pharmacological Research, Agenzia Italiana del Farmaco
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1. Study Identification

Unique Protocol Identification Number
NCT01257672
Brief Title
Symptomatic Treatment of Acute Gastroenteritis
Official Title
Oral Ondansetron vs Domperidone for Symptomatic Treatment of Vomiting During Acute Gastroenteritis in Children: Multicentre Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
November 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS Burlo Garofolo
Collaborators
Mario Negri Institute for Pharmacological Research, Agenzia Italiana del Farmaco

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroenteritis, Vomiting, Acute Gastroenteritis
Keywords
acute gastroenteritis, vomiting, ondansetron, domperidon, symptomatic treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
356 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ondansetron
Arm Type
Experimental
Arm Description
ondansetron, syrup, 0,15 mg/Kg of body weight, 1 dose
Arm Title
domperidon
Arm Type
Active Comparator
Arm Description
domperidone, syrup, 0,5 mg/Kg of body weight, one dose
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo, syrup, one dose
Intervention Type
Drug
Intervention Name(s)
Ondansetron
Other Intervention Name(s)
zofran
Intervention Description
ondansetron syrup (0,15 mg/Kg of body weight)
Intervention Type
Drug
Intervention Name(s)
Domperidone
Other Intervention Name(s)
Motilium
Intervention Description
domperidone syrup (0,5 mg/Kg of body weight)
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
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
Secondary Outcome Measure Information:
Title
Percentage of subjects needing hospital admission for the same illness;
Time Frame
48 hours
Title
Percentage of subjects needing observation stay for more than 6 hours for the same illness
Time Frame
48 hours
Title
Total emesis duration in the 3 allocation groups;
Time Frame
48 hours
Title
Number of episodes of vomiting in the 3 treatment groups during the follow-up period
Time Frame
48 hours
Title
Percentage of subjects presenting adverse events
Time Frame
48 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age from 1 to 6 years; presumptive clinical diagnosis of acute gastroenteritis in patients with vomiting, with or without diarrhoea; more than three episodes of non-bilious, non-bloody vomiting within the previous 24 hours; Exclusion Criteria: treatment with antiemetics or antidiarrhoic drugs in the 6 hours prior to access to ED; underlying chronic diseases (eg, malignancy, gastroesophageal reflux, migraine, renal failure, hypoalbuminemia, liver disease); severe dehydration: weight loss>10% or standardized clinical dehydration score >=18 for children aged 12-24 months and >=16 for older children; known hypersensitivity to ondansetron or domperidone; previous enrolment in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Federico Marchetti, MD
Organizational Affiliation
IRCCS Burlo Garofolo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maurizio Bonati, MD
Organizational Affiliation
Mario Negri Institute for Pharmacological Research
Official's Role
Study Director
Facility Information:
Facility Name
Dipartimento di Pediatria, Ospedale Castelli
City
Verbania
State/Province
Novara
Country
Italy
Facility Name
Dipartimento di Emergenza Pediatrica, Ospedale Giuseppe Moscati
City
Avellino
Country
Italy
Facility Name
Dipartimento di Emergenza Pediatrica, P.O. Spedali Civili
City
Brescia
Country
Italy
Facility Name
Divisione di Emergenza Pediatrica, Ospedale Pediatrico A. Meyer
City
Firenze
Country
Italy
Facility Name
Unità Operativa di Pediatria, Ospedale GB Morgagni
City
Forlì
Country
Italy
Facility Name
Divisione di Emergenza Pediatrica, Istituto G. Gaslini
City
Genova
Country
Italy
Facility Name
Dipartimento di Pediatrica, Ospedale di Macerata
City
Macerata
Country
Italy
Facility Name
Dipartimento di Pediatria, Azienda Policlinico di Modena
City
Modena
Country
Italy
Facility Name
Dipartimento di Emergenza Pediatrica, Azienda Ospedaliera - Università di Padova
City
Padova
Country
Italy
Facility Name
Dipartimento di Pediatrica, Azienda Ospedaliera- Università di Parma
City
Parma
Country
Italy
Facility Name
Dipartimento di Emergenza Pediatrica, Ospedale Pediatrico IRCCS Bambino Gesú
City
Roma
Country
Italy
Facility Name
Dipartimento di Emergenza Pediatrica, Ospedale Infantile Regina Margherita
City
Torino
Country
Italy
Facility Name
Dipartimento di Pediatria, Ospedale di Treviso
City
Treviso
Country
Italy
Facility Name
Dipartimento di Emergenza Pediatrica, Istituto per la l'Infanzia, IRCCS Burlo Garofolo
City
Trieste
Country
Italy
Facility Name
Unità di Terapia Intensiva Pediatrica, Ospedale Civile Maggiore
City
Verona
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
21310051
Citation
Marchetti F, Maestro A, Rovere F, Zanon D, Arrighini A, Bertolani P, Biban P, Da Dalt L, Di Pietro P, Renna S, Guala A, Mannelli F, Pazzaglia A, Messi G, Perri F, Reale A, Urbino AF, Valletta E, Vitale A, Zangardi T, Tondelli MT, Clavenna A, Bonati M, Ronfani L. Oral ondansetron versus domperidone for symptomatic treatment of vomiting during acute gastroenteritis in children: multicentre randomized controlled trial. BMC Pediatr. 2011 Feb 10;11:15. doi: 10.1186/1471-2431-11-15.
Results Reference
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Symptomatic Treatment of Acute Gastroenteritis

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