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Search / Trial NCT04782817

Reducing Reintubation Risk in High-Risk Cardiac Surgery Patients With High-Flow Nasal Cannula

Launched by VANDERBILT UNIVERSITY MEDICAL CENTER · Mar 1, 2021

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

High Flow Nasal Cannula Oxygen Therapy Reintubation

ClinConnect Summary

This clinical trial is studying how to reduce the chances of needing to put a breathing tube back in (reintubation) for patients who have just undergone heart surgery. The researchers want to compare two groups of patients: one group will receive oxygen therapy using high-flow nasal cannulas (which are soft tubes that deliver oxygen through the nose), while the other group will receive the usual care chosen by their healthcare team. The goal is to see which method leads to better outcomes after surgery.

To be eligible for this study, participants need to be adults aged 18 and older who have had heart surgery that lasted at least three hours and were on a breathing machine when they arrived at the intensive care unit. They also need to be expected to have their breathing tube removed at some point while in the unit. Those who meet these criteria will have the opportunity to help researchers understand how to improve care for heart surgery patients. Participants can expect to be monitored closely during their recovery and may experience different methods of receiving oxygen as part of the trial.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Age ≥18 years
  • Undergoing cardiac surgery, defined as a documented surgical service of "cardiac surgery" in the electronic health record, performed in the main operating rooms at Vanderbilt University Medical Center
  • Admitted to the cardiovascular intensive care unit postoperatively with an endotracheal tube in place and mechanically ventilated
  • Surgery duration (documented time between "Anesthesia start" and "Anesthesia stop" in the EHR) of at least 180 minutes
  • Received an order to be extubated by a treating provider o Patients who meet all other criteria but do not receive an order to extubate will be randomized but not enrolled
  • Exclusion Criteria
  • • Patient does not meet inclusion criteria

About Vanderbilt University Medical Center

Vanderbilt University Medical Center (VUMC) is a leading academic medical center located in Nashville, Tennessee, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a prominent sponsor of clinical trials, VUMC integrates cutting-edge scientific inquiry with patient-centered care, supporting a diverse array of studies aimed at enhancing medical knowledge and improving treatment outcomes. With a robust infrastructure and a multidisciplinary team of experts, VUMC fosters collaboration across various fields, ensuring the highest standards of safety and ethical considerations in its research endeavors. Through its dedication to medical discovery and education, VUMC plays a pivotal role in shaping the future of medicine.

Locations

Nashville, Tennessee, United States

Patients applied

0 patients applied

Trial Officials

Robert E Freundlich, MD

Principal Investigator

Vanderbilt University Medical Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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