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Variation in Fluids Administered in Shock (VOLUME)

Montefiore Medicine Academic Health System logo

Montefiore Medicine Academic Health System

Status

Completed

Conditions

Shock

Treatments

Other: Fluids

Study type

Observational

Funder types

Other

Identifiers

NCT03190408
2017-7860

Details and patient eligibility

About

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.

Enrollment

1,639 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

1,639 participants in 1 patient group

Shock
Treatment:
Other: Fluids

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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