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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00147849
Date of registration: 02/09/2005
Primary sponsor: Canadian Institutes of Health Research (CIHR)
Public title: A Cluster Controlled Trial Comparing Three Methods of Disseminating Practice Guidelines for Children With Croup
Scientific title: A Cluster Controlled Trial Comparing Three Methods of Disseminating Practice
Date of first enrolment: September 2000
Target sample size:
Recruitment status: Terminated
URL:  http://clinicaltrials.gov/show/NCT00147849
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Educational/Counseling/Training  
Countries of recruitment
Contacts
Name:   David W Johnson, MD
Address: 
Telephone:
Email:
Affiliation:  University of Calgary
Key inclusion & exclusion criteria

Inclusion Criteria:

- Alberta hospitals were rank ordered based on the number of disease episodes and rates
of hospitalization for a six-year period. We then approached in this order each of
the hospital administrators and clinical staff for permission to include their
hospital in our study until a total of 24 hospitals consented

Exclusion Criteria:

- Refusal by hospital staff to participate in this trial



Age minimum: N/A
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Croup
Intervention(s)
Behavioral: a combination of interactive educational meetings, educational outreach visits, and reminders
Behavioral: identification of local opinion leaders and establishment of local consensus processes
Behavioral: mailing of printed educational materials
Primary Outcome(s)
Rate of hospital days per 1,000 disease episodes
Secondary Outcome(s)
An economic analysis conducted from a societal perspective with costs classified as either payer (costs born by the province) or non-payer (costs born by individuals or the families of children with croup).
Proportion of patients evaluated in ED for at least three hours after treatment with corticosteroids before the decision to admit to hospital is made.
Proportion of patients treated in the ED and hospital with a corticosteroid.
Time to treatment with corticosteroids in both ED and hospital patients.
Secondary ID(s)
CIHR App No. 110642
MCT-63141
U Calgary Acct. No. 73-1051
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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