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Efficacy Study of IV Fluids Only vs Ondansetron to Treat Dehydration

Primary Purpose

Dehydration, Gastroenteritis

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ondansetron
Saline
Sponsored by
Children's Hospitals and Clinics of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dehydration focused on measuring dehydration, acute gastroenteritis, ondansetron, rehydration

Eligibility Criteria

6 Months - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 6 months - 5 years
  • Clinical diagnosis of acute gastroenteritis
  • Mild or moderate dehydration as determined by validated clinical scale
  • Clinical assessment to begin IV fluids
  • Vomiting ≥ 2 episodes in past 4 hours

Exclusion Criteria:

  • Severe dehydration
  • History of significant gastrointestinal, metabolic, renal or cardiac disorder
  • Ondansetron allergy
  • Non-English language proficient parent/guardian
  • Parent/guardian has no telephone

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Active Comparator

    Arm Label

    2

    1

    Arm Description

    Saline

    Zofran

    Outcomes

    Primary Outcome Measures

    Received further IV fluids

    Secondary Outcome Measures

    Full Information

    First Posted
    June 3, 2008
    Last Updated
    July 13, 2015
    Sponsor
    Children's Hospitals and Clinics of Minnesota
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00691275
    Brief Title
    Efficacy Study of IV Fluids Only vs Ondansetron to Treat Dehydration
    Official Title
    Ondansetron vs. Placebo in the Management of Children With Dehydration Due to Acute Gastroenteritis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2015
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    September 2008 (undefined)
    Primary Completion Date
    September 2009 (Anticipated)
    Study Completion Date
    September 2009 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Children's Hospitals and Clinics of Minnesota

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Dehydration due to vomiting is a common complication of acute gastroenteritis in children. Persistent vomiting following rehydration is a problem in outpatient management using oral rehydration therapy. Four previous studies have examined the role of the medication, ondansetron, in treating nausea and vomiting in children with gastroenteritis and have suggested that it may be beneficial [1-4]. A previous study has also shown that the administration of intravenous fluid alone to children with dehydration due to gastroenteritis helps resolve nausea and vomiting in the majority of patients [5]. None of the previous studies compared the efficacy of intravenous ondansetron with that of intravenous fluid alone in the prevention of vomiting . In addition, the previous studies were limited by poorly defined inclusion criteria and outcome measures. The proposed study seeks to more clearly define the role of intravenous ondansetron in the management of children suffering dehydration due to acute gastroenteritis. If ondansetron further reduces the incidence of vomiting compared with intravenous fluid alone, more children with dehydration due to acute gastroenteritis may be successfully discharged to home from the emergency department instead of admitted to the hospital. If it does not, the widespread use of ondansetron for such patients could be discouraged and money could be saved. Hypothesis: Patients receiving ondansetron in addition to intravenous fluids for the treatment of dehydration due to vomiting caused by gastroenteritis will not have a significant reduction in the occurrence of persistent vomiting as compared to those who receive only intravenous fluids.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Dehydration, Gastroenteritis
    Keywords
    dehydration, acute gastroenteritis, ondansetron, rehydration

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    2
    Arm Type
    Placebo Comparator
    Arm Description
    Saline
    Arm Title
    1
    Arm Type
    Active Comparator
    Arm Description
    Zofran
    Intervention Type
    Drug
    Intervention Name(s)
    Ondansetron
    Intervention Type
    Drug
    Intervention Name(s)
    Saline
    Primary Outcome Measure Information:
    Title
    Received further IV fluids
    Time Frame
    2-7 days post discharge

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Months
    Maximum Age & Unit of Time
    5 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 6 months - 5 years Clinical diagnosis of acute gastroenteritis Mild or moderate dehydration as determined by validated clinical scale Clinical assessment to begin IV fluids Vomiting ≥ 2 episodes in past 4 hours Exclusion Criteria: Severe dehydration History of significant gastrointestinal, metabolic, renal or cardiac disorder Ondansetron allergy Non-English language proficient parent/guardian Parent/guardian has no telephone
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Sam Reid, MD
    Organizational Affiliation
    Children's Hospitals and Clinics of Minnesota
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Henry Ortega, MD
    Organizational Affiliation
    Children's Hospitals and Clinics of Minnesota
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Jeffrey Louie, MD
    Organizational Affiliation
    Children's Hospitals and Clinics of Minnesota
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    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.
    Results Reference
    background
    PubMed Identifier
    11927735
    Citation
    Reeves JJ, Shannon MW, Fleisher GR. Ondansetron decreases vomiting associated with acute gastroenteritis: a randomized, controlled trial. Pediatrics. 2002 Apr;109(4):e62. doi: 10.1542/peds.109.4.e62.
    Results Reference
    background
    PubMed Identifier
    11919526
    Citation
    Ramsook C, Sahagun-Carreon I, Kozinetz CA, Moro-Sutherland D. A randomized clinical trial comparing oral ondansetron with placebo in children with vomiting from acute gastroenteritis. Ann Emerg Med. 2002 Apr;39(4):397-403. doi: 10.1067/mem.2002.122706.
    Results Reference
    background
    PubMed Identifier
    16902049
    Citation
    Stork CM, Brown KM, Reilly TH, Secreti L, Brown LH. Emergency department treatment of viral gastritis using intravenous ondansetron or dexamethasone in children. Acad Emerg Med. 2006 Oct;13(10):1027-33. doi: 10.1197/j.aem.2006.05.018. Epub 2006 Aug 10.
    Results Reference
    background
    PubMed Identifier
    8780476
    Citation
    Reid SR, Bonadio WA. Outpatient rapid intravenous rehydration to correct dehydration and resolve vomiting in children with acute gastroenteritis. Ann Emerg Med. 1996 Sep;28(3):318-23. doi: 10.1016/s0196-0644(96)70032-x.
    Results Reference
    background

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    Efficacy Study of IV Fluids Only vs Ondansetron to Treat Dehydration

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