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Rapid Treatment of Shock Without Trauma

NCT05073354 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 27

Last updated 2024-07-24

No results posted yet for this study

Summary

Evaluate the implementation of a standardized mobile resuscitation model to manage SWOT within a large acute care hospital setting.

Conditions

  • Shock

Interventions

DEVICE

Full SWOT Model

Bundle of care that includes devices such as X Series monitor/defibrillator, AutoPusle automated compression device, Z Vent ventilator, and IPR therapies as well as bedside monitoring and diagnostics and training on a standardized care process.

Sponsors & Collaborators

  • Zoll Medical Corporation

    lead INDUSTRY

Principal Investigators

  • Tonia M Mowbray-Donahue, MD · Allina Health

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-29
Primary Completion
2024-04-05
Completion
2024-04-05
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05073354 on ClinicalTrials.gov