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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02754947
Other study ID # IRB14-00946
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 2015
Est. completion date March 2016

Study information

Verified date December 2023
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study was to identify the etiology of events and demographics of patients that experience complications requiring activation of the Rapid Response Team (RRT) during the first 24 h following anesthetic care.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date March 2016
Est. primary completion date February 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Any study subject that experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility. Exclusion Criteria: - Any study subject that has not experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility.

Study Design


Locations

Country Name City State
United States Nationwide Children's Hospital Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Nationwide Children's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Identifying post-operative criteria for activation of Rapid Response Teams (RRTs) in caring for the pediatric population using Pediatric Early Warning Scores (PEWS) To retrospectively identify the etiologies associated with a need to engage Rapid Response Teams (RRTs) to promote frequent assessments and early interventions among clinically deteriorating hospitalized pediatric patients. 24 hours post-operatively
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