NCT02754947

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2015

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2015

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2016

Completed
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2016

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

April 25, 2016

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 28, 2016

Completed
Last Updated

December 13, 2023

Status Verified

December 1, 2023

Enrollment Period

1 year

First QC Date

April 25, 2016

Last Update Submit

December 7, 2023

Conditions

Cardiovascular DiseasesRespiratory DiseasesNeurologic Diseases

Keywords

Assessment and Consultation Team (ACT)Rapid Response Team (RRT)Perioperative complicationsRespiratory insufficiencyASA status

Outcome Measures

Primary Outcomes (1)

  • 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

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Any study subject that experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility reviewed from an existing Department of Anesthesiology \& Pain Medicine database.

You may qualify if:

  • Any study subject that experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility.

You may not qualify if:

  • Any study subject that has not experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nationwide Children's Hospital

Columbus, Ohio, 43205, United States

Location

MeSH Terms

Conditions

Cardiovascular DiseasesRespiratory Tract DiseasesNervous System DiseasesRespiratory Insufficiency

Condition Hierarchy (Ancestors)

Respiration Disorders

Study Officials

  • N'Diris Barry, BS, RN, MSN

    Nationwide Children's Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 25, 2016

First Posted

April 28, 2016

Study Start

February 1, 2015

Primary Completion

February 1, 2016

Study Completion

March 1, 2016

Last Updated

December 13, 2023

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations

US(1)