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NCT02164851 · ClinicalTrials.gov registry record
Non-Invasive Shock: Differentiating Shock in the Emergency Department
A clinical trial, sponsored by Beth Israel Deaconess Medical Center.
- Completed
- Registry status
- 500
- Enrollment target
NCT02164851: Completed study, sponsored by Beth Israel Deaconess Medical Center.
NCT02164851 is a clinical trial that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 500 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02164851 has completed, sponsored by Beth Israel Deaconess Medical Center.
- COMPLETED
- Registry status
- 500 participants
- Enrollment target
Study Summary
The goal of this study is to compare the characteristics of echocardiography and different monitoring devices in shock patients, the relationship of device parameters to biomarkers associated with shock, and determine if these any of these add clinical utility when predicting the cause of shock. We will perform a prospective, observational study of patients found to have shock physiology in the ED and follow them to determine the final shock category and ultimate outcomes.
Primary Outcome
Composite in hospital endpoint: 1) acute renal failure (Creatinine 2x baseline or new hemodialysis), non-elective intubation, vasopressor requirement, mortality.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 500 participants |
| Start Date | 2012-11-28 |
| Est. Completion | 2020-01-01 |
What the finished NCT02164851 record still lists
NCT02164851 is an observational study that tracks outcomes without assigning an intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT02164851 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02164851 about?
NCT02164851 is a clinical study titled "Non-Invasive Shock: Differentiating Shock in the Emergency Department". The goal of this study is to compare the characteristics of echocardiography and different monitoring devices in shock patients, the relationship of device parameters to biomarkers associated with shock, and determine if these any of these add clinical utility when predicting the cause of shock. We ...
What is the current status of trial NCT02164851?
This trial is currently completed. The enrollment target is 500 participants. The study started on 2012-11-28. Estimated completion is 2020-01-01.
Who is sponsoring clinical trial NCT02164851?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
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