Antiemetic Efficacy of Ondansetron Versus Metoclopramide
Primary Purpose
Acute Gastroenteritis, Vomiting
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Ondansetron
metoclopramide
Sponsored by
About this trial
This is an interventional treatment trial for Acute Gastroenteritis focused on measuring vomiting in children, ondansetron, metoclopramide, antiemetics
Eligibility Criteria
Inclusion Criteria:
- Orally intolerance
- More than 2 vomiting in the last 24 hours
- Without antiemetic therapy within 24 hours of the clinical picture
- Patients with or without diarrhea
Exclusion Criteria:
- Previous abdominal surgery
- Suspected surgical abdominal
- Vomiting bile
- Hypersensitivity to Ondansetron and Metoclopramide
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
ondansetron
metoclopramide
Arm Description
An intravenous dose of ondansetron ( 0.15mg /kg / doses ) Diluted in 20 ml of saline and administer intravenously in 5 minutes
An intravenous dose of metoclopramide ( 0.15mg /kg / doses ) Diluted in 20 ml of saline and administer intravenously in 5 minutes
Outcomes
Primary Outcome Measures
Cumulative rate of vomiting after cessation of drug administration
Secondary Outcome Measures
Full Information
NCT ID
NCT02619201
First Posted
November 25, 2015
Last Updated
November 30, 2015
Sponsor
Hospital General Naval de Alta Especialidad - Escuela Medico Naval
1. Study Identification
Unique Protocol Identification Number
NCT02619201
Brief Title
Antiemetic Efficacy of Ondansetron Versus Metoclopramide
Official Title
Comparison of Efficacy of Ondansetron Versus Metoclopramide for Vomiting in Children With Acute Gastroenteritis: Randomized Controlled Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
November 2015 (undefined)
Primary Completion Date
May 2016 (Anticipated)
Study Completion Date
November 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital General Naval de Alta Especialidad - Escuela Medico Naval
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Acute gastroenteritis (GEA) is a public health problem at present, the main cause of vomiting and consultation in emergencies in children under 5 years. Worldwide, there are about 2 million deaths per year due to gastroenteritis in children under 5 years.
In Mexico, the mortality rate by age in 2013, recorded 28 deaths per 100,000 boys and girls, in 2013 in our country 2.5 million children between 5 and 17 years engaged in an economic activity. The occupancy rate for the child population was 8.6: 11.4 for boys and 5.8 for girls.
NICE guidance gastroenteritis defined as a transient disorder caused by an enteric infection and characterized by a sudden onset of diarrhea with or without vomiting
Detailed Description
It will be conducted a randomized controlled double-blinded study in the Emergency service of the Naval General Hospital of High Specialty in the Mexico City. The period of patient inclusion in the study is November 2015 to November 2016.
The selections of the patients are children between 1 and 5 years who come to the emergency room with symptoms of acute gastroenteritis with vomiting and intolerance of oral route.
Treatments were randomly assigned eligible patients on admission in the emergency department
The primary endpoint was evaluated at 15 minutes after treatment application:
Treatment 1: Ondansetron was administered intravenous dose (0.15mg/kg/doses) Diluted in 20 ml saline and administered intravenously 5 minutes
Treatment 2: Metoclopramide was administered intravenous dose (0.15mg/kg/doses) Diluted in 20 ml saline and administered intravenously 5 minutes
The administration of intravenous medications, will be held in the observation area of the emergency department of pediatrics under monitoring continuo vital signs during application and 15 minutes after treatment.
At 15 minutes after administration, the mouth with oral electrolyte begins by assessing your tolerance, 30 minutes to progress to the astringent diet.
It will follow up with patient assessment in the emergency department of pediatrics, 3 hours after having established the treatment, in order to corroborate the remission of vomiting, it is graduation of home otherwise he will enter hospital.
Primary objective Cumulative rate of cessation of vomiting
secondary objectives
Compare the number of vomiting episodes with the administration of ondansetron vs metoclopramide
Compare time duration in which the oral route is restarted.
Compare hospital admission rate
Describe adverse effects in both groups
Inclusion Criteria:
Orally intolerance
More than 2 vomiting in the last 24 hours
Without antiemetic therapy within 24 hours of the clinical picture
Patients with or without diarrhea
Exclusion Criteria:
Previous abdominal surgery
Suspected surgical abdominal
vomiting bile
Hypersensitivity to Ondansetron and Metoclopramide
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Gastroenteritis, Vomiting
Keywords
vomiting in children, ondansetron, metoclopramide, antiemetics
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
250 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
ondansetron
Arm Type
Experimental
Arm Description
An intravenous dose of ondansetron ( 0.15mg /kg / doses ) Diluted in 20 ml of saline and administer intravenously in 5 minutes
Arm Title
metoclopramide
Arm Type
Active Comparator
Arm Description
An intravenous dose of metoclopramide ( 0.15mg /kg / doses ) Diluted in 20 ml of saline and administer intravenously in 5 minutes
Intervention Type
Drug
Intervention Name(s)
Ondansetron
Other Intervention Name(s)
OD
Intervention Description
An intravenous dose of ondansetron ( 0.15mg /kg / doses ) .
Intervention Type
Drug
Intervention Name(s)
metoclopramide
Other Intervention Name(s)
MT
Intervention Description
An intravenous dose of metoclopramide ( 0.15mg /kg / doses ) .
Primary Outcome Measure Information:
Title
Cumulative rate of vomiting after cessation of drug administration
Time Frame
4 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Orally intolerance
More than 2 vomiting in the last 24 hours
Without antiemetic therapy within 24 hours of the clinical picture
Patients with or without diarrhea
Exclusion Criteria:
Previous abdominal surgery
Suspected surgical abdominal
Vomiting bile
Hypersensitivity to Ondansetron and Metoclopramide
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yaneth Miranda Tecuautzin, medicine
Phone
66 91 60 07 39
Email
missin1821@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jose de Jesus Gutierrez Escobedo, medicine
Phone
5516910741
Email
abi2228@msn.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yaneth Miranda Tecuautzin, medicine
Organizational Affiliation
Secretaria de Marina-Armada de México (Mexican Navy)
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
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12211601
Citation
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Results Reference
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PubMed Identifier
22132432
Citation
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Antiemetic Efficacy of Ondansetron Versus Metoclopramide
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