Variation in Fluids Administered in Shock
Completed
- Conditions
- Shock
- Interventions
- Other: Fluids
- Registration Number
- NCT03190408
- Lead Sponsor
- Montefiore Medical Center
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1639
Inclusion Criteria
- 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
Exclusion Criteria
- 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.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Shock Fluids -
- Primary Outcome Measures
Name Time Method Method used to guide volume resuscitation 7 days Characterize the method used to guide volume resuscitation and vasopressor use in patients with shock
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Montefiore Medical Center
🇺🇸Bronx, New York, United States