Cardiac Arrest Clinical Trials

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Critical Health Assessment and Outcomes Score/Study

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

CHAOS is based on the investigator's new and exciting results from pre-clinical and large longitudinal multi-center observational clinical studies of critically ill patients and asymptomatic community-based adults with little or no advanced disease. By integrating approaches from the physical, biological, computational, statistical and clinical sciences, this observational study will test the hypothesis that early diagnosis of subclinical signatures of critical illness encoded within physiological signals complements conventional clinical predictors by providing unique prognostic insight. The primary goal is to reduce mortality, morbidity and complications by early identification of individuals with brewing subclinical critical illness and adverse events before overt clinical presentation (e.g., cardiac arrest, arrhythmias, hemorrhage, respiratory failure, circulatory collapse). This will provide the necessary lead time for healthcare providers to deliver early, more effective and/or preventive therapies. Through innovative approaches, CHAOS also meets the challenge of medical errors to reduce missed diagnosis, misdiagnosis, preventable harm and variability in provider adherence to best practice guidelines. The goal is to validate predictive algorithms and identify subclinical signatures of illness, ranging from asymptomatic adults in the community to very sick patients in the hospital. The overall goal is to make healthcare more precise, effective, efficient, safe and timely while reducing costs, preventable harms and adverse events.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• All patients age 18-100 years admitted to a bed or OR with telemetry monitoring capability will be included.

Locations
United States
Indiana
Indiana University
NOT_YET_RECRUITING
Indianapolis
Maryland
Johns Hopkins University
NOT_YET_RECRUITING
Baltimore
Ohio
University of Cincinnati
RECRUITING
Cincinnati
Contact Information
Primary
Deeptankar DeMazumder, MD, PhD
DDeMazu@iu.edu
513-558-1035
Backup
Deeptankar DeMazumder, MD, PhD
Deeptankar@gmail.com
513-558-1035
Time Frame
Start Date: 2019-09-01
Estimated Completion Date: 2027-09-01
Participants
Target number of participants: 200000
Treatments
Predictive Monitoring
No Predictive Monitoring
Related Therapeutic Areas
Sponsors
Collaborators: Indiana University, University of Cincinnati
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov