Inpatient Mortality Prediction Algorithm Clinical Trial (IMPACT)

Sponsor
Dascena (Industry)
Overall Status
Withdrawn
CT.gov ID
NCT03212534
Collaborator
University of California, San Francisco (Other)
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Study Details

Study Description

Brief Summary

Through the mapping of retrospective patient data into a discrete multidimensional space, a novel algorithm for homeostatic analysis, was built to make outcome predictions. In this prospective study, the ability of the algorithm to predict patient mortality and influence clinical outcomes, will be investigated.

Condition or Disease Intervention/Treatment Phase
  • Other: Patient mortality prediction
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
A Randomized Clinical Trial of a Mortality Prediction Algorithm
Anticipated Study Start Date :
Jul 1, 2017
Anticipated Primary Completion Date :
Oct 1, 2017
Anticipated Study Completion Date :
Oct 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Prediction Algorithm

Other: Patient mortality prediction
Healthcare provider is notified of patient mortality prediction.

No Intervention: Control

Outcome Measures

Primary Outcome Measures

  1. In-hospital mortality [Through study completion, an average of 30 days]

Secondary Outcome Measures

  1. Hospital length of stay [Through study completion, an average of 30 days]

Other Outcome Measures

  1. Hospital readmission [Through study completion, an average of 30 days]

  2. ICU length of stay [Through study completion, an average of 30 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All adult patients admitted to the participating units will be eligible.
Exclusion Criteria:
  • All patients younger than 18 years of age will be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCSF Moffit-Long Hospital San Francisco California United States 94143

Sponsors and Collaborators

  • Dascena
  • University of California, San Francisco

Investigators

  • Principal Investigator: David Shimabukuro, University of California, San Francisco

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dascena
ClinicalTrials.gov Identifier:
NCT03212534
Other Study ID Numbers:
  • 17-22319
First Posted:
Jul 11, 2017
Last Update Posted:
Sep 24, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dascena
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 24, 2021