Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03288311 · ClinicalTrials.gov registry record · NA

Protocolized Post-Extubation Respiratory Support Study

A NA study, sponsored by Vanderbilt University Medical Center.

Completed
Registry status
NA
Development phase
751
Enrollment target

NCT03288311: Completed NA study, sponsored by Vanderbilt University Medical Center.

NCT03288311 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 751 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03288311, a NA study, has completed, sponsored by Vanderbilt University Medical Center.

COMPLETED
Registry status
NA
Development phase
751 participants
Enrollment target

Study Summary

Invasive mechanical ventilation is common in the medical intensive care unit, and the period of time following extubation remains high risk as 11 to 15% of patients require reintubation after their first extubation. Reintubation is associated with increased rates of nosocomial infection and is an independent predictor of mortality. Non-invasive ventilation and high flow nasal cannula are the only therapies that have been shown to reduce the rate of reintubation. Recent clinical trials suggest that all patients might benefit from some form of post-extubation respiratory support, but use of these therapies in usual care remains low. PROPER is a cluster-randomized, multiple-crossover trial comparing a respiratory therapist driven protocol to provide post-extubation respiratory support to all patients, compared to usual care. The trial will enroll patients undergoing extubation in the Medical ICU at Vanderbilt from October 2017 until March 2019. The primary outcome will be reintubation within 96 hours.

Primary Outcome

Any placement of an endotracheal tube for any indication within 96 hours of extubation, censored at the first of hospital discharge or 96 hours after extubation

Interventions

  • OTHER Usual Care
  • OTHER Protocolized post-extubation respiratory support

Trial Details

FieldValue
Enrollment Target 751 participants
Start Date 2017-10-01
Est. Completion 2019-04-28
Phase NA

What the finished NCT03288311 record still lists

NCT03288311 is an interventional study that assigns participants to a tested intervention. The registered 751 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 2 interventions - of which Usual Care is the first listed.

NCT03288311 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03288311 about?

NCT03288311 is a clinical study titled "Protocolized Post-Extubation Respiratory Support Study". Invasive mechanical ventilation is common in the medical intensive care unit, and the period of time following extubation remains high risk as 11 to 15% of patients require reintubation after their first extubation. Reintubation is associated with increased rates of nosocomial infection and is an in...

What is the current status of trial NCT03288311?

This trial is currently completed. It is a NA study. The enrollment target is 751 participants. The study started on 2017-10-01. Estimated completion is 2019-04-28.

What interventions are being tested in trial NCT03288311?

The interventions under investigation include: Usual Care (OTHER), Protocolized post-extubation respiratory support (OTHER).

Who is sponsoring clinical trial NCT03288311?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03288311's enrollment target sits among peer trials

751 145th of 2000 higher than 1,856 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT06559306 · 752 participants · Phase 3

    Phase 3 Study of Adjunctive Treatment With Seltorexant in Adult and Elderly Participants With Major Depressive Disorder and Insomnia Symptoms

  • NCT02048332 · 750 participants · Phase 1

    Donor-Derived Viral Specific T-cells (VSTs)

  • NCT02087852 · 750 participants

    Kidney Cancer DNA Registry

  • NCT02532452 · 750 participants · Phase 2

    Third Party Viral Specific T-cells (VSTs)

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03288311, the US trial registry maintained by the National Library of Medicine. NCT03288311 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.