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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
Hospital General Naval de Alta Especialidad - Escuela Medico Naval
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Gastroenteritis focused on measuring vomiting in children, ondansetron, metoclopramide, antiemetics

Eligibility Criteria

1 Year - 5 Years (Child)All SexesDoes not accept healthy volunteers

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

    First Posted
    November 25, 2015
    Last Updated
    November 30, 2015
    Sponsor
    Hospital General Naval de Alta Especialidad - Escuela Medico Naval
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    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:
    PubMed Identifier
    12211601
    Citation
    Herikstad H, Yang S, Van Gilder TJ, Vugia D, Hadler J, Blake P, Deneen V, Shiferaw B, Angulo FJ. A population-based estimate of the burden of diarrhoeal illness in the United States: FoodNet, 1996-7. Epidemiol Infect. 2002 Aug;129(1):9-17. doi: 10.1017/s0950268801006628.
    Results Reference
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    PubMed Identifier
    18493225
    Citation
    Guarino A, Albano F, Ashkenazi S, Gendrel D, Hoekstra JH, Shamir R, Szajewska H; ESPGHAN/ESPID Evidence-Based Guidelines for the Management of Acute Gastroenteritis in Children in Europe Expert Working Group. European Society for Paediatric Gastroenterology, Hepatology, and Nutrition/European Society for Paediatric Infectious Diseases evidence-based guidelines for the management of acute gastroenteritis in children in Europe: executive summary. J Pediatr Gastroenterol Nutr. 2008 May;46(5):619-21. doi: 10.1097/MPG.0b013e31816e219e. No abstract available.
    Results Reference
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    PubMed Identifier
    6689452
    Citation
    Haque KN, al-Frayh A, el-Rifai R. Is it necessary to regraduate milk after acute gastroenteritis in children? Trop Geogr Med. 1983 Dec;35(4):369-73.
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    PubMed Identifier
    22815462
    Citation
    Carter B, Fedorowicz Z. Antiemetic treatment for acute gastroenteritis in children: an updated Cochrane systematic review with meta-analysis and mixed treatment comparison in a Bayesian framework. BMJ Open. 2012 Jul 19;2(4):e000622. doi: 10.1136/bmjopen-2011-000622. Print 2012.
    Results Reference
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    PubMed Identifier
    22132432
    Citation
    National Collaborating Centre for Women's and Children's Health (UK). Diarrhoea and Vomiting Caused by Gastroenteritis: Diagnosis, Assessment and Management in Children Younger than 5 Years. London: RCOG Press; 2009 Apr. Available from http://www.ncbi.nlm.nih.gov/books/NBK63844/
    Results Reference
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    PubMed Identifier
    19550407
    Citation
    Atia AN, Buchman AL. Oral rehydration solutions in non-cholera diarrhea: a review. Am J Gastroenterol. 2009 Oct;104(10):2596-604; quiz 2605. doi: 10.1038/ajg.2009.329. Epub 2009 Jun 23.
    Results Reference
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    PubMed Identifier
    16625009
    Citation
    Freedman SB, Adler M, Seshadri R, Powell EC. Oral ondansetron for gastroenteritis in a pediatric emergency department. N Engl J Med. 2006 Apr 20;354(16):1698-705. doi: 10.1056/NEJMoa055119.
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    PubMed Identifier
    24171058
    Citation
    Rerksuppaphol S, Rerksuppaphol L. Randomized study of ondansetron versus domperidone in the treatment of children with acute gastroenteritis. J Clin Med Res. 2013 Dec;5(6):460-6. doi: 10.4021/jocmr1500w. Epub 2013 Oct 12.
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    PubMed Identifier
    24564795
    Citation
    Das JK, Kumar R, Salam RA, Freedman S, Bhutta ZA. The effect of antiemetics in childhood gastroenteritis. BMC Public Health. 2013;13 Suppl 3(Suppl 3):S9. doi: 10.1186/1471-2458-13-S3-S9. Epub 2013 Sep 17.
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    PubMed Identifier
    18006189
    Citation
    Roslund G, Hepps TS, McQuillen KK. The role of oral ondansetron in children with vomiting as a result of acute gastritis/gastroenteritis who have failed oral rehydration therapy: a randomized controlled trial. Ann Emerg Med. 2008 Jul;52(1):22-29.e6. doi: 10.1016/j.annemergmed.2007.09.010. Epub 2007 Nov 19. Erratum In: Ann Emerg Med. 2008 Oct;52(4):406.
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    Antiemetic Efficacy of Ondansetron Versus Metoclopramide

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