Variation in Fluids Administered in Shock

Completed

Conditions studied: Shock

In brief

To conduct a multicenter observational cohort study to determine the variability in fluid resuscitation in shock in a broad range of areas in hospitals and treatment areas.

Key facts

Study ID

NCT03190408

Run by

Montefiore Medical Center

People needed

1639

Starts

2017-09-01

Expected to finish

2018-02-01

Last updated by the study team

2020-07-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years admitted to the participating hospital.
• Patients in the emergency department, intensive care unit, PACU, or any hospital floor. For patients not in the ICU, there must be plans to transfer to an intensive care unit when an ICU bed is available for patient.
• Patients with shock as defined by:
• Need for vasopressor (dopamine, norepinephrine, or epinephrine at any dose) to keep MAP > 65 mmHg Or
• Systolic BP < 90 mmHg

You may not qualify if…

• Patients previously enrolled into this study.
• Patients who were in the operating room at time of shock and fluid bolus.
• Patients admitted to an ICU after cardiac surgery Patients with primarily cardiogenic shock as etiology for their shock
• Patients transferred from another hospital or emergency room to the study hospital.

Where it is running

• Montefiore Medical Center — The Bronx, New York, United States

Full record on ClinicalTrials.gov

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