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Oral Prednisolone Dosing in Children Hospitalized With Asthma

23 december 2010 bijgewerkt door: Children's Hospital of Philadelphia
This study hopes to determine the appropriate oral steroid dose for treating children hospitalized with asthma exacerbations. Practice guidelines from different countries recommend a wide range of doses, and the doses used in actual practice vary widely. There is no data on what is the most appropriate dose of prednisone (or equivalent) in this situation. We will be looking at the dose recommended by the National Asthma Education and Prevention Program guidelines, which are published by the National Heart, Lung, and Blood Institute, as compared with a lower dose which is commonly used in practice. We hypothesize that the lower dose will be no worse than the higher dose as determined primarily by duration of hospitalization.

Studie Overzicht

Gedetailleerde beschrijving

Practice guidelines for the management of asthma in children universally recommend systemic corticosteroids for the treatment of moderate to severe asthma exacerbations. However, these guidelines vary widely with respect to dose, frequency, method of delivery, and duration of therapy. In actual practice, there is also considerable variation among clinicians in terms of corticosteroid dosing in children hospitalized with asthma exacerbations. At the Children's Hospital of Philadelphia (CHOP) the current standard is to use an initial dose of 4.0 mg/kg/day (1.0 mg/kg every 6 hours to a maximum of 30 mg/dose) although many other pediatric hospitals use a 2.0 mg/kg/day dose (1.0 mg/kg every 12 hours to a maximum of 30 mg/dose). Systematic reviews of the literature have called for a clinical trial to evaluate the effect of different doses of corticosteroids in treating pediatric asthma patients hospitalized with exacerbations.

This study will use a randomized, double-blind, controlled trial design in order to compare the efficacy of two different steroid doses in resolving acute exacerbations of asthma in hospitalized children. Children being hospitalized for asthma exacerbations from the CHOP emergency department (ED) will be eligible for study enrollment. Those that meet enrollment criteria will be randomized to receive prednisolone either in the higher dose (1.0 mg/kg (max 30 mg) every 6 hours), or the lower dose (1.0 mg/kg (max 30 mg) every 12 hours and placebo doses at 6 hour intervals in between) for the first 48 hours of hospitalization. Once 48 hours has past, all patients still hospitalized will receive 1.0 mg/kg (max 30 mg) every 12 hours for the duration of hospitalization. Approximately 156 patients with 78 in each arm of the study will be enrolled. This study should be completed in six to eight months. A non-inferiority study design will be used. The primary outcome will be duration of hospitalization, as determined by duration of time elapsed from first dose of prednisolone administered in the emergency department (ED) until the discharge dose of albuterol is administered. Secondary outcomes will include time elapsed from the time the admission order is written until the discharge order is written, time spent in each severity level of the asthma care pathway, degree and rate of improvement in forced expiratory volume in one second (FEV1), improvement in peak expiratory flows (PEF), improvement in asthma symptom scores, and rate of relapse after discharge.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

152

Fase

  • Fase 4

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Pennsylvania
      • Philadelphia, Pennsylvania, Verenigde Staten, 19104
        • The Children's Hospital of Philadelphia

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

2 jaar tot 18 jaar (Kind, Volwassen)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Physician-diagnosed asthma with at least two previous visits to ED or primary care provider for asthma care
  • Clinical decision by ED attending physician to admit to Acute Care Unit (ACU) after standardized initial ED treatment

Exclusion Criteria:

  • Clinical decision to begin continuous intravenous beta-agonist infusion
  • Clinical decision to begin intravenous methylprednisolone therapy
  • Clinical decision to admit to the Pediatric Intensive Care Unit
  • Other concurrent disease such as sickle cell disease, cystic fibrosis, or cardiac disease
  • Any contraindication to corticosteroid administration
  • Any systemic corticosteroid treatment within two weeks of presenting to the ED
  • Potential subjects will be excluded if informed consent is not obtained

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Actieve vergelijker: 1
High dose prednisolone
4 mg/kg/day orally divided every 6 hours (maximum 30 mg per dose)
Andere namen:
  • corticosteroïden
  • High Dose Prednisolone
  • Oral steriod
  • asthma exacerbations
Experimenteel: 2
Lower dose prednisolone alternating with placebo
2 mg/kg/day orally divided q 12 (maximum 30mg/dose) alternating with placebo
Andere namen:
  • corticosteroïden
  • Oral steriod
  • asthma exacerbations
  • Low dose Prednisolone
  • Oral prednisolone

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Time Measured From the Administration of the Loading Dose of Prednisolone (2mg/kg up to Max 60mg) in the Emergency Department (ED) Until the Home Dose of Albuterol is Administered
Tijdsspanne: Median time from loading dose to home dose of albuterol
Median time from loading dose to home dose of albuterol

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Time Measured From the Writing of the Admission Order Until the Writing of the Discharge Order
Tijdsspanne: Mean time from writing admit order until discharge order
Mean time from writing admit order until discharge order
Time Spent in Each Severity Level of the Asthma Care Pathway
Tijdsspanne: Time spent in each severity level of pathway
Time spent in each severity level of pathway
The Rate and Degree of Change in Forced Expiratory Volume (FEV1) and Peak Expiratory Flow (PEF) Between Treatment Groups
Tijdsspanne: Every 4 hours during hospitalization
Every 4 hours during hospitalization
Differences in Clinical Asthma Symptom Scores During Hospitalization Between Treatment Groups
Tijdsspanne: Every 4 hours during hospitalization
Every 4 hours during hospitalization
Rate of Relapse Between Treatment Groups
Tijdsspanne: 2 weeks after hospitalization
2 weeks after hospitalization

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Joseph J Zorc, MD, Children's Hospital of Philadelphia

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 februari 2006

Primaire voltooiing (Werkelijk)

1 november 2006

Studie voltooiing (Werkelijk)

1 november 2006

Studieregistratiedata

Eerst ingediend

22 november 2005

Eerst ingediend dat voldeed aan de QC-criteria

22 november 2005

Eerst geplaatst (Schatting)

24 november 2005

Updates van studierecords

Laatste update geplaatst (Schatting)

31 december 2010

Laatste update ingediend die voldeed aan QC-criteria

23 december 2010

Laatst geverifieerd

1 december 2010

Meer informatie

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