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The Acute Burn Resuscitation Multicenter Prospective Observational Trial

NCT03144427 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2021-07-21

No results posted yet for this study

Summary

This is a prospective, non-interventional, observational study of consecutive burn patients admitted to 20 selected burn centers in North America. Primarily, data collection will be continuous "real-time" documentation of fluid infusion rates, vital signs and laboratory values of patients receiving fluid resuscitation during the first 48 hours following burn injury. All aspects of the resuscitation and all investigations performed will be according to the participating center's regular protocol, as this is purely an observational and non-interventional study. Further data collection on outcomes (organ function, ventilation duration, length of stay, and survival) will be collected at 72h, 96 h, and at hospital discharge.

Conditions

  • Burns
  • Shock

Sponsors & Collaborators

  • U.S. Army Medical Research Acquisition Activity

    collaborator FED

  • University of California, Davis

    collaborator OTHER

  • American Burn Association

    lead OTHER

Principal Investigators

  • David Greenhalgh, MD · University of California, Davis

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-24
Primary Completion
2021-07-15
Completion
2021-07-15

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 NCT03144427 on ClinicalTrials.gov