Shock Clinical Trial
— VOLUMEOfficial title:
Observation of Variation in Fluids Administered and Characterization of Vasopressor Requirements in Shock
Verified date | July 2020 |
Source | Montefiore Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 1639 |
Est. completion date | February 1, 2018 |
Est. primary completion date | February 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
United States | Montefiore Medical Center | Bronx | New York |
Lead Sponsor | Collaborator |
---|---|
Montefiore Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Method used to guide volume resuscitation | Characterize the method used to guide volume resuscitation and vasopressor use in patients with shock | 7 days |
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