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Clinical Trials/NCT02497729
NCT02497729CompletedPhase 4

Checklists and Upright Positioning in Endotracheal Intubation of Critically Ill Patients (Check-UP) Trial

Vanderbilt University10 sites in 1 country260 target enrollmentStarted: July 2015Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
260
Locations
10
Primary Endpoint
Lowest Systolic Blood Pressure (Checklist intervention only)

Study Overview

Brief Summary

The use of a written, pre-procedure checklist and positioning the patient with the head of the bed elevated have been proposed as interventions capable of preventing complications during non-elective intubation and are used intermittently in routine care -- however neither have been examined in a prospective trial.

Detailed Description

Endotracheal intubation is common in the care of critically ill patients. Procedural complications including hypoxia and hypotension are frequent in urgent and emergent intubation and associated with an increased risk of death. The use of a written, pre-procedure checklist and positioning the patient with the head of the bed elevated have been proposed as interventions capable of preventing complications during non-elective intubation and are used intermittently in routine care -- however neither have been examined in a prospective trial. The investigators propose a randomized trial comparing use of a written checklist versus no written checklist and ramped versus sniffing position for endotracheal intubation of critically ill adults.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Airway management events will be included in which:
  • Patient is admitted to the Medical Intensive Care Unit (MICU)
  • Planned procedure is endotracheal intubation
  • Planned operator is a Pulmonary and Critical Care Medicine (PCCM) fellow
  • Administration of sedation and/or neuromuscular blockade is planned
  • Age ≥ 18 years old

Exclusion Criteria

  • Airway management events will be excluded in which:
  • Operator feels specific patient positioning during intubation is required
  • Urgency of intubation precludes safe performance of study procedures
  • Operator feels an alternative pre-procedure checklist or no checklist is required

Outcomes

Primary Outcomes

Lowest Systolic Blood Pressure (Checklist intervention only)

Time Frame: Time of Induction through 2 minutes after successful intubation

Lowest non-invasively or invasively measured systolic blood pressure between medication administration and 2 minutes following successful placement of an endotracheal tube (in checklist comparison only)

Lowest Arterial Oxygen Saturation (Both positioning and Checklist interventions)

Time Frame: Time of Induction through 2 minutes after successful intubation

Lowest non-invasively measured arterial oxygen saturation between the time of induction or neuromuscular blockade and two minutes after completion of the airway management procedure

Secondary Outcomes

  • Grade of First Glottic View(Time of Induction through 2 minutes after successful intubation)
  • First Pass Success(Time of Induction through 2 minutes after successful intubation)
  • Time to Intubation(Time of Induction through 2 minutes after successful intubation)
  • Number of Intubation Attempts(Time of Induction through 2 minutes after successful intubation)
  • Repositioning Patient(Time of Induction through 2 minutes after successful intubation)
  • Incidence of Hypoxemia(Time of Induction through 2 minutes after successful intubation)
  • Malposition of Endotracheal Tube(Time of Induction through 2 minutes after successful intubation)
  • Change in Saturation(Time of Induction through 2 minutes after successful intubation)
  • Non-hypoxic complications(Time of Induction through 2 minutes after successful intubation)
  • In-Hospital Mortality(From enrollment through the earlier of hospital discharge or 365 days)
  • Incidence of Desaturation(Time of Induction through 2 minutes after successful intubation)
  • Need for Assistance(Time of Induction through 2 minutes after successful intubation)
  • Ventilator-free Days(From enrollment through study day 28)
  • ICU-Free Days(From enrollment through study day 28)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Todd Rice

Associate Professor of Medicine

Vanderbilt University

Study Sites (10)

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