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Main
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Note: This record shows only 22 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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02398981 |
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Date of registration:
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13/02/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Implementation of a Web Based Real Time Clinical Decision Support Tool.
CERTAINp |
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Scientific title:
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Design and Pilot Implementation of a Web Based Real Time Clinical Decision Support Tool. (Checklist for Early Recognition and Treatment of Acute Illness in Pediatrics. CERTAINp |
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Date of first enrolment:
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February 2015 |
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Target sample size:
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962 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02398981 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized. Intervention model: Single Group Assignment. Primary purpose: Supportive Care. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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China
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Congo
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Croatia
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Fiji
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India
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Peru
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All pediatric patients (< 18 years) admitted for the first time to the participating
PICUs will be included.
Exclusion Criteria:
- Not critically ill, admitted for low risk monitoring, planned PICU admission for
routine post operative surveillance for less than 24 hours after uncomplicated
surgery, readmission and transfer from outside PICU.
Age minimum:
N/A
Age maximum:
17 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Shock
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Bleeding
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Sepsis
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Critical Illness
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Respiratory Failure
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Intervention(s)
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Other: Clinical decision support tool
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Primary Outcome(s)
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ICU and hospital lengths of stay
[Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 8 weeks]
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Secondary Outcome(s)
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Adherence to best critical care practices as measured by composite measures of best practice guidelines.
[Time Frame: Participants will be followed for the duration of ICU stay, an expected average of 2 weeks]
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Secondary ID(s)
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14-004429
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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