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NCT03190408 Clinical Trial

Variation in Fluids Administered in Shock

Shock Clinical Trial

— VOLUME  

Official title:
Observation of Variation in Fluids Administered and Characterization of Vasopressor Requirements in Shock

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03190408
Other study ID # 2017-7860
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2017
Est. completion date February 1, 2018

Study information
Verified date July 2020
Source Montefiore Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
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.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Fluids
Fluids Administered in Shock

Locations
Country Name City State
United States Montefiore Medical Center Bronx New York

Sponsors (1)
Lead Sponsor Collaborator
Montefiore Medical Center

Country where clinical trial is conducted

United States, 

Outcome
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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