Effect of Early Transition to Assisted Ventilation on 28-day Successful Extubation in Critically Ill Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSoutheast University, China

About this trial

EARLY-VENT is a multicenter, open-label, three-period cluster-randomized crossover trial designed to evaluate whether early transition from controlled to assisted ventilation improves outcomes in critically ill patients. The study will enroll approximately 1,600 adult patients across 10 ICUs who are expected to require mechanical ventilation for at least 48 hours and meet specific stability criteria (e.g., hemodynamically stable, light sedation). Participating centers will alternate between an experimental strategy, where patients transition to an assisted mode (preferably Pressure Support Ventilation) within 6 hours of eligibility, and a control strategy based on standard care practices. The primary endpoint is the rate of successful extubation at day 28, aiming to demonstrate that transition from controlled to assisted ventilation can reduce ventilation duration and improve prognosis compared to delayed transition.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years.

Expected ICU stay and mechanical ventilation (MV) ≥ 48 hours.

Currently receiving controlled ventilation mode

No neuromuscular blocking agents in use, and sedation level RASS ≥ -3.

Disqualifiers

Severe end-stage irreversible respiratory, cardiac, or neurologic disease that may lead to long-term/chronic ventilator dependence or inability to wean from MV (e.g., interstitial lung disease/pulmonary fibrosis, cardiomyopathy, valvular disease, severe traumatic brain injury, Guillain-Barré syndrome, amyotrophic lateral sclerosis, multiple sclerosis, high cervical spinal cord injury, or other restrictive diseases).

Expected death or transfer out of the ICU within 48 hours.

Hemodynamic instability judged by the treating clinician.

Pregnancy.

Trial design

Design model

Crossover

Treatments tested in this trial

  • Early Transition

    Behavioral

    Patients are transitioned from controlled to assisted ventilation (preferably Pressure Support Ventilation) within 6 hours of meeting the eligibility criteria

Treatment groups

1,600 Participants
are divided into 2 treatment groups
Group A: early transitionExperimental treatment 1 intervention
Group B: standard careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

the rate of successful extubation at day 28

1. No re-intubation or death occurred for 7 consecutive days after extubation, or the patient survived ICU admission with non-invasive mechanical ventilation within 7 days post-extubation-whichever occurs first. 2. For tracheostomy patients: Successful extubation is defined as achieving spontaneous ventilation through the tracheostomy for seven consecutive days without any form of assisted ventilation, or discharge from the ICU without assisted respiratory support, whichever occurs first.

Time frame
the rate of successful extubation at day 28

Secondary outcomes

Other outcomes

Sponsors and contacts

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