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Search / Trial NCT02118467

Vasoactive Drugs in Intensive Care Unit

Launched by UNIVERSITY OF CHICAGO · Apr 16, 2014

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Shock Vasopressor Agents Norepinephrine Epinephrine Phenylephrine Vasopressin Atrial Fibrillation Tachyarrhythmia

ClinConnect Summary

This clinical trial, titled "Vasoactive Drugs in Intensive Care Unit," is studying how different medications can help patients in the Intensive Care Unit (ICU) who are experiencing shock, a serious condition where the body doesn’t get enough blood flow. The researchers want to find out if using the medications phenylephrine and vasopressin is better at preventing irregular heartbeats (called tachydysrhythmias) compared to norepinephrine and epinephrine, which are commonly used in these situations. The trial is currently recruiting patients aged 18 and older who need these medications to treat shock that hasn’t improved with fluids.

If you or a loved one are eligible to participate, you will be randomly assigned to receive one of the two treatment options. The study is designed to compare the effects of these medications on your condition, and you will not know which treatment you are receiving, which helps ensure the results are unbiased. It’s important to know that this trial is focused on patients who have low blood pressure despite receiving fluids, and some conditions, such as severe heart failure or being pregnant, may prevent participation. Your healthcare team can provide more information and help determine if this study is appropriate for you.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Age greater than or equal to 18 years old
  • 2. Requirement for vasoactive drugs via a central venous catheter for the treatment of shock. Shock will be defined as mean arterial pressure less than 70 mmHg or systolic blood pressure less than 100 mmHg despite administration of at least 1000 mL of crystalloid or 500 mL of colloid, unless there is an elevation in the central venous pressure to \> 12 mmHg or in the pulmonary artery occlusion pressure to \> 14 mmHg coupled with signs of tissue hypoperfusion (e.g. altered mental state, mottled skin, urine output \< 0.5 mL/kg body weight for one hour, or a serum lactate level of \> 2 mmol per liter).
  • Exclusion Criteria:
  • 1. Cardiopulmonary arrest
  • 2. Pregnancy
  • 3. Severe right heart failure

About University Of Chicago

The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

John P Kress, MD

Principal Investigator

University of Chicago

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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