Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT02118467

Vasoactive Drugs in Intensive Care Unit

Led by University of Chicago · Updated on 2026-01-13

836

Participants Needed

1

Research Sites

654 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators hypothesis is that for ICU patients with shock, the use of the vasoactive drugs phenylephrine and vasopressin will reduce tachydysrhythmias when compared to norepinephrine and epinephrine. To investigate this hypothesis, the investigators are conducting a randomized double blind controlled trial comparing phenylephrine and vasopressin vs. norepinephrine and epinephrine in ICU patients with shock that is not responsive to IV fluids. All patients admitted to the adult intensive care units at the University of Chicago will be screened for eligibility.

CONDITIONS

Official Title

Vasoactive Drugs in Intensive Care Unit

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than or equal to 18 years old
  • Need for vasoactive drugs via a central venous catheter to treat shock defined by low blood pressure despite receiving at least 1000 mL of crystalloid or 500 mL of colloid fluids unless elevated pressures and signs of poor tissue blood flow are present
Not Eligible

You will not qualify if you...

  • Cardiopulmonary arrest
  • Pregnancy
  • Severe right heart failure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Chicago Medical Center

Chicago, Illinois, United States, 60637

Actively Recruiting

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Research Team

J

John P Kress, MD

CONTACT

A

Anne Pohlman

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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