RECRUITING

Optimal Timing for Spontaneous Breathing Trials

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study aims to explore how the timing of Spontaneous Breathing Trials (SBTs) affects recovery in adult patients who are on mechanical ventilation in the ICU. SBTs are tests used to determine if a patient is ready to breathe on their own without the help of a ventilator. The study will compare two different timing strategies for these trials: one group of patients will have the test early in the morning, while the other group will have it later in the morning. By observing the outcomes, such as how long patients need to stay on the ventilator, the study hopes to find the best time to perform these trials to help patients recover more quickly and safely.

Official Title

Impact of Spontaneous Breathing Trial Timing on Outcomes in Mechanically Ventilated Adult Patients

Quick Facts

Study Start:2024-09-17
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06561295

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults aged 21 years or older.
  2. * Patients who have been on mechanical ventilation for more than 48 hours.
  3. * Patients who have completed at least one SBT.
  1. * Patients intubated at other hospitals.
  2. * Patients intubated for surgical or interventional procedures.
  3. * Patients receiving venovenous extracorporeal membrane oxygenation (VV-ECMO).
  4. * Patients with a tracheostomy.

Contacts and Locations

Study Contact

JIE LI, PhD
CONTACT
3125634643
jie_li@rush.edu

Principal Investigator

JIE LI, PhD
PRINCIPAL_INVESTIGATOR
Rush University

Study Locations (Sites)

Rush University Medical Center
Chicago, Illinois, 60612
United States

Collaborators and Investigators

Sponsor: Rush University Medical Center

  • JIE LI, PhD, PRINCIPAL_INVESTIGATOR, Rush University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-17
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2024-09-17
Study Completion Date2026-06-30

Terms related to this study

Keywords Provided by Researchers

  • Spontaneous breathing trial
  • Weaning
  • Mechanical ventilation duration

Additional Relevant MeSH Terms

  • Respiration, Artificial
  • Weaning