TOOLs: Titration of Oxygen Levels During Mechanical Ventilation With Electronic Alerts

Sponsor
Ohio State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04481581
Collaborator
National Center for Advancing Translational Science (NCATS) (NIH)
300
1
2
18.8
16

Study Details

Study Description

Brief Summary

Fractional oxygen during mechanical ventilation, is a life sustaining therapy in the intensive care unit , used for about a million patients annually. Oxygen therapy needs to be tightly balanced as both hypoxia and hyperoxia are harmful. Establishing precision in oxygenation has significant implications for improving patient outcomes, resource utilization and reducing iatrogenic harm to a vulnerable population. The investigators propose an approach using a oxygen titration protocol consisting of electronic health records based alerts to guide oxygen adjustment.

Condition or Disease Intervention/Treatment Phase
  • Other: Electronic Alerts
Phase 3

Detailed Description

The investigators will conduct a prospective randomized, clinical trial in the Medical Intensive Care Unit at Ohio State University Medical Center. In the intervention arm, respiratory therapists' will conduct oxygen titration with the help of a novel, high fidelity, electronic health records based, protocol consisting of electronic alerts and decision support tool. Oxygen titration in the control arm will be done without alerts and will be per "current standard of care".

Participants for this study will be identified and recruited from patients admitted to the Ohio State University, Wexner Medical Center and James Cancer Hospital, Medical Intensive Care Unit.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This will be a parallel design, unblinded, randomized (1:1) trialThis will be a parallel design, unblinded, randomized (1:1) trial
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
In this study providers cannot be masked, outcome assessors and investigators will be blinded
Primary Purpose:
Treatment
Official Title:
Titration of Inspired Oxygen During Mechanical Ventilation Using a Bedside Decision Support Tool
Actual Study Start Date :
Jan 5, 2021
Anticipated Primary Completion Date :
Jan 30, 2022
Anticipated Study Completion Date :
Jul 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention arm- Oxygen titration with electronic alerts

Oxygen titration will be done based on electronic alerts and decisions support tool by Respiratory Therapists, if FiO2=> 0.4 and SpO2 =>94% for more than 45 minutes

Other: Electronic Alerts
When FiO2 remains =>0.4 and SpO2 =>94% for more than 45 minutes, an electronic health record based alert will be sent to respiratory therapists to titrate oxygen per decision support tool.

No Intervention: Control Arm- Oxygen titration by one time physician orders

Oxygen titration will be done ventilator management guidelines for the medical intensive care unit. Titration is done by one-time orders.

Outcome Measures

Primary Outcome Measures

  1. Duration of Hyperoxemia [Duration of Mechanical Ventilation, an average of 10-14 days]

    The degree of excess exposure will be recorded as percent FiO2 >0.4 when saturation continued to remain above 94%. Primary outcome will be determined by the proportion of time the patient will be "exposed to excessive supplied oxygen" divided by the total time under mechanical ventilation.

Secondary Outcome Measures

  1. Ventilator Free days [28 days]

    The number of days between successful weaning from mechanical ventilation and day 28 after study enrollment.

  2. ICU length of stay [days of ICU stay within hospitalization, average of 20-25 days]

    Duration of stay in the intensive care unit after patient enrollment

  3. Duration of stay in the hospital after patient enrollment [Current Hospital Stay, upto 30 days]

    Duration of stay in the hospital after patient enrollment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

• Critically ill subjects who require mechanical ventilation for at least 24 hours.

Exclusion Criteria:
  • Subjects without research authorization,

  • Pregnancy,

  • Pneumothorax,

  • Carbon monoxide poisoning,

  • Hyperbaric oxygen therapy

  • Acute ST elevation Myocardial Infarction

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ohio State University Medical Center Columbus Ohio United States 43210

Sponsors and Collaborators

  • Ohio State University
  • National Center for Advancing Translational Science (NCATS)

Investigators

  • Principal Investigator: Sonal R Pannu, M.D., Ohio State University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sonal Pannu, Assistant Professor, Ohio State University
ClinicalTrials.gov Identifier:
NCT04481581
Other Study ID Numbers:
  • 2014H0236
  • 5KL2TR002734-03
First Posted:
Jul 22, 2020
Last Update Posted:
Jan 27, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 27, 2021