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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02184208
Other study ID # IRB-P000011819
Secondary ID
Status Completed
Phase N/A
First received July 2, 2014
Last updated July 18, 2017
Start date January 17, 2014
Est. completion date January 9, 2017

Study information

Verified date July 2017
Source Boston Children’s Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Today, the electronic medical record, microprocessor mechanical ventilators, and physiologic monitoring are under-utilized when translating research into decision support. Current medical informatic capabilities can be leveraged to calculate trends in measured parameters to initiate a paradigm shift in critical care from reaction-based treatment to proactive and plausibly preventative care. Therefore, the purpose of this study is to develop baseline understanding of our practice and how data collection utilizing a newly implemented system called T3. We would like to retrospectively review mechanically ventilated patients in which we have collected continuous data to test a newly developed analytic platform. Additionally we would like to compare these results to our standards of practice established by clinical practice guidelines.


Recruitment information / eligibility

Status Completed
Enrollment 278
Est. completion date January 9, 2017
Est. primary completion date December 30, 2016
Accepts healthy volunteers No
Gender All
Age group N/A to 35 Years
Eligibility Inclusion Criteria:

- Patient selection will be determined by available data collected in the T3 system. We estimate 50 patients in which mechanical ventilator data has been collected utilizing the limited intellibridge modules (4 systems currently available to collect ventilator data).

Exclusion Criteria:

- Patient not connected to T3 data collection system.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Boston Children's Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Boston Children’s Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Successful Extubation Successful extubation without the use of noninvasive ventilation or requiring reintubation Within 24 hours of extubation
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