search
Back to results

High Flow Nasal Cannula With Noninvasive Ventilation

Primary Purpose

Acute Respiratory Failure

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Standard of Care - Nasal Cannula
High-flow nasal cannula
HFNC plus non-invasive ventilation
Sponsored by
University of Oklahoma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Failure focused on measuring acute respiratory failure, mechanical ventilation

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Adults at least 18 years of age
  2. Admission to an intensive care unit by the trauma surgery service
  3. Trauma patients receiving any respiratory therapies
  4. High risk patients, including intubation, post-operative, chronic cardiac or pulmonary comorbidities
  5. Thoracic injuries, including rib fractures, sternal fractures, spinal fractures, pulmonary contusions, pneumothorax, hemothorax, diaphragm injury
  6. Postoperative from thoracic surgery
  7. Postoperative from spine surgery in patients without spinal cord injury
  8. Abdominal injuries requiring open abdominal surgery
  9. No contraindications to using high flow nasal cannula or noninvasive ventilation

Exclusion Criteria:

  1. Contraindication to using high flow nasal cannula or noninvasive ventilation
  2. Intolerance of pulmonary therapies
  3. No one able to give informed consent
  4. Long-term treatment with noninvasive ventilation prior to hospital admission
  5. "Do not intubate" order at time of extubation
  6. Unplanned extubation (accidental or self-extubation)
  7. Age < 18 years of age
  8. Traumatic brain injury with GCS < 8
  9. Spinal cord injury
  10. Chronic neuromuscular disease
  11. Sinus precautions due to facial/sinus fractures

Sites / Locations

  • OU Medical CenterRecruiting
  • OU Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Not Intubated

Intubated Patients Undergoing Extubation

Arm Description

Patients admitted with a trauma injury who do not need to be intubated to receive treatment. Intubated means putting a tube down your throat to keep your airway from collapsing. Participants will be randomized to receive one of the three interventions in this arm.

Patients admitted with a trauma injury who had to be intubated for treatment of their injury. Interventions administered after the tube is extubated (removed from throat). Participants will be randomized to receive one of the three interventions in this arm.

Outcomes

Primary Outcome Measures

failure rates-nonintubated patients
Among injured patients admitted to the intensive care unit (ICU) without being intubated, do failure rates within the first 48 hours of ICU admission differ with respect to type of initial respiratory intervention: nasal cannula, high-flow nasal cannula (HFNC), or HFNC plus non-invasive ventilation (BiPAP). Failure is defined as escalation to intubation.
failure rates-intubated patients
Among injured patients arriving intubated or who undergo intervention after hospital arrival, do failure rates within the first 48 hours after extubation differ with respect to type of initial respiratory intervention: nasal cannula, high-flow nasal cannula (HFNC), or HFNC plus non-invasive ventilation (BiPAP). Failure is defined as requiring reintubation.

Secondary Outcome Measures

Mortality
Assess mortality of enrolled patients by quarterly retrospective chart reviews.
Length of hospital stay
Compare length of hospitalization between groups
Length of ICU stay
Compare length of ICU stay between groups
Discharge location
was patient discharged to home, rehabilitation facility, skilled nursing, death; compare between groups
Complications
Compare complications (such as need to be mechanically ventilated, infections, etc.) between groups

Full Information

First Posted
July 25, 2020
Last Updated
April 11, 2022
Sponsor
University of Oklahoma
search

1. Study Identification

Unique Protocol Identification Number
NCT04507425
Brief Title
High Flow Nasal Cannula With Noninvasive Ventilation
Official Title
High Flow Nasal Cannula With Noninvasive Ventilation and Its Effect on High Risk Trauma Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oklahoma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a prospective, randomized, unblinded trial of trauma patients in the ICU who are identified as being at a high risk to develop acute respiratory failure. We hope that this study will help the study team to identify how best to use a more aggressive respiratory treatment strategy in a high risk trauma population (thoracic trauma or trauma patients requiring thoracic surgery, spine surgery, or open abdominal procedures) to try and decrease the need for intubation with mechanical ventilation.
Detailed Description
All patients consented will be randomly assigned into one of three groups: nasal cannula (control group, our current standard of care), high-flow nasal cannula, high-flow nasal cannula plus noninvasive ventilation. After obtaining consent, patient will be randomized to interventions 1:1:1 within each of two groups: patients admitted to the ICU without being intubated OR intubated patients undergoing an extubation. Randomization will be managed through RedCap. After consent, the treating clinician will log into RedCap to obtain the patient's treating assignment. The primary outcome of interest is failure of conservative ventilation intervention in prevention of initial intubation or prevention of reintubation. A chart review of all enrolled patients will be done quarterly to assess morbidity, mortality, and outcomes. No placebo will be used as all qualifying patients will be placed on nasal cannula, high-flow nasal cannula, or high-flow nasal cannula plus noninvasive ventilation. All other treatments will be standard of care. Participants in the study will continue until the patient is discharged from the trauma ICU. The study will end when the last person enrolled has been discharged from the trauma ICU. If patient's participation ends prematurely, available data will be entered into the database and evaluated appropriately. This study will take place at the OU Medical Center (OUMC) among patients admitted to the Trauma Intensive Care Unit. Consent for study enrollment will take place at OUMC during discussion with physician providing trauma care and the patient, family member, or next of kin consenting for the study. The following data will be collected and recorded: Supplemental oxygen requirements, Date/Time of arrival, Date/Time of Admission to ICU, Date/Time of intubation procedure, Date/Time of extubation, Ventilator settings, Duration of intubation, Comorbidities, PaCO2 values, PaO2 values, Vital signs at arrival and at admission to ICU, Age,Gender, Weight, Height, BMI, Traumatic injuries, Diagnosis, Past medical history/medical co-morbidities, Glasgow coma scale, Oxygen saturation, Negative inspiratory force score, Rapid shallow breathing index score, Pulmonary treatments, including an intolerance to therapy, Injury Severity Score (ISS) and/or Abbreviated Injury Scale (AIS).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Failure
Keywords
acute respiratory failure, mechanical ventilation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized into 1 of 3 interventions: nasal cannula, high flow nasal cannula, and high flow nasal cannula plus noninvasive ventilation within each of two groups: patients admitted to ICU without being intubated OR intubated patients undergoing an extubation.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1770 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Not Intubated
Arm Type
Active Comparator
Arm Description
Patients admitted with a trauma injury who do not need to be intubated to receive treatment. Intubated means putting a tube down your throat to keep your airway from collapsing. Participants will be randomized to receive one of the three interventions in this arm.
Arm Title
Intubated Patients Undergoing Extubation
Arm Type
Active Comparator
Arm Description
Patients admitted with a trauma injury who had to be intubated for treatment of their injury. Interventions administered after the tube is extubated (removed from throat). Participants will be randomized to receive one of the three interventions in this arm.
Intervention Type
Other
Intervention Name(s)
Standard of Care - Nasal Cannula
Intervention Description
Standard of care. Flexible tube to provide extra oxygen when patients need a little help, but are not in respiratory distress.
Intervention Type
Other
Intervention Name(s)
High-flow nasal cannula
Other Intervention Name(s)
HFNC
Intervention Description
Same as nasal cannula, except the oxygen is heated or humidified and the flow is stronger, pushing air into the lungs to help keep the airway open.
Intervention Type
Other
Intervention Name(s)
HFNC plus non-invasive ventilation
Intervention Description
This method uses HFNC as described above and adds noninvasive ventilation which is similar to CPAP machine and uses a mask rather than having to intubate (putting a tube down your throat to keep your airway from collapsing).
Primary Outcome Measure Information:
Title
failure rates-nonintubated patients
Description
Among injured patients admitted to the intensive care unit (ICU) without being intubated, do failure rates within the first 48 hours of ICU admission differ with respect to type of initial respiratory intervention: nasal cannula, high-flow nasal cannula (HFNC), or HFNC plus non-invasive ventilation (BiPAP). Failure is defined as escalation to intubation.
Time Frame
first 48 hours
Title
failure rates-intubated patients
Description
Among injured patients arriving intubated or who undergo intervention after hospital arrival, do failure rates within the first 48 hours after extubation differ with respect to type of initial respiratory intervention: nasal cannula, high-flow nasal cannula (HFNC), or HFNC plus non-invasive ventilation (BiPAP). Failure is defined as requiring reintubation.
Time Frame
first 48 hours
Secondary Outcome Measure Information:
Title
Mortality
Description
Assess mortality of enrolled patients by quarterly retrospective chart reviews.
Time Frame
Up to 2 years
Title
Length of hospital stay
Description
Compare length of hospitalization between groups
Time Frame
up to 60 days
Title
Length of ICU stay
Description
Compare length of ICU stay between groups
Time Frame
up to 30 days
Title
Discharge location
Description
was patient discharged to home, rehabilitation facility, skilled nursing, death; compare between groups
Time Frame
up to 60 days
Title
Complications
Description
Compare complications (such as need to be mechanically ventilated, infections, etc.) between groups
Time Frame
up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults at least 18 years of age Admission to an intensive care unit by the trauma surgery service Trauma patients receiving any respiratory therapies High risk patients, including intubation, post-operative, chronic cardiac or pulmonary comorbidities Thoracic injuries, including rib fractures, sternal fractures, spinal fractures, pulmonary contusions, pneumothorax, hemothorax, diaphragm injury Postoperative from thoracic surgery Postoperative from spine surgery in patients without spinal cord injury Abdominal injuries requiring open abdominal surgery No contraindications to using high flow nasal cannula or noninvasive ventilation Exclusion Criteria: Contraindication to using high flow nasal cannula or noninvasive ventilation Intolerance of pulmonary therapies No one able to give informed consent Long-term treatment with noninvasive ventilation prior to hospital admission "Do not intubate" order at time of extubation Unplanned extubation (accidental or self-extubation) Age < 18 years of age Traumatic brain injury with GCS < 8 Spinal cord injury Chronic neuromuscular disease Sinus precautions due to facial/sinus fractures
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Theresa Lander
Phone
405-271-2601
Ext
2
Email
theresa-lander@ouhsc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Asaleigh Cline
Phone
405-271-8001
Ext
56021
Email
asaleigh-cline@ouhsc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Celia Y Quang, MD
Organizational Affiliation
University of Oklahoma
Official's Role
Principal Investigator
Facility Information:
Facility Name
OU Medical Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Celia Quang, MD
Phone
405-271-8001
Ext
55004
Email
celia-quang@ouhsc.edu
Facility Name
OU Medical Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Theresa Lander
Phone
405-271-2601
Ext
43230
Email
theresa-lander@ouhsc.edu
First Name & Middle Initial & Last Name & Degree
Stephanie Mitchell, RN
Phone
405-271-2128
Email
Stephanie-mitchell@ouhsc.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26926168
Citation
Thille AW, Boissier F, Ben-Ghezala H, Razazi K, Mekontso-Dessap A, Brun-Buisson C, Brochard L. Easily identified at-risk patients for extubation failure may benefit from noninvasive ventilation: a prospective before-after study. Crit Care. 2016 Feb 26;20:48. doi: 10.1186/s13054-016-1228-2.
Results Reference
result
PubMed Identifier
31577036
Citation
Thille AW, Muller G, Gacouin A, Coudroy R, Decavele M, Sonneville R, Beloncle F, Girault C, Dangers L, Lautrette A, Cabasson S, Rouze A, Vivier E, Le Meur A, Ricard JD, Razazi K, Barberet G, Lebert C, Ehrmann S, Sabatier C, Bourenne J, Pradel G, Bailly P, Terzi N, Dellamonica J, Lacave G, Danin PE, Nanadoumgar H, Gibelin A, Zanre L, Deye N, Demoule A, Maamar A, Nay MA, Robert R, Ragot S, Frat JP; HIGH-WEAN Study Group and the REVA Research Network. Effect of Postextubation High-Flow Nasal Oxygen With Noninvasive Ventilation vs High-Flow Nasal Oxygen Alone on Reintubation Among Patients at High Risk of Extubation Failure: A Randomized Clinical Trial. JAMA. 2019 Oct 15;322(15):1465-1475. doi: 10.1001/jama.2019.14901. Erratum In: JAMA. 2020 Feb 25;323(8):793.
Results Reference
result
PubMed Identifier
30326893
Citation
Xu Z, Li Y, Zhou J, Li X, Huang Y, Liu X, Burns KEA, Zhong N, Zhang H. High-flow nasal cannula in adults with acute respiratory failure and after extubation: a systematic review and meta-analysis. Respir Res. 2018 Oct 16;19(1):202. doi: 10.1186/s12931-018-0908-7.
Results Reference
result
PubMed Identifier
16354864
Citation
Honrubia T, Garcia Lopez FJ, Franco N, Mas M, Guevara M, Daguerre M, Alia I, Algora A, Galdos P. Noninvasive vs conventional mechanical ventilation in acute respiratory failure: a multicenter, randomized controlled trial. Chest. 2005 Dec;128(6):3916-24. doi: 10.1378/chest.128.6.3916.
Results Reference
result
PubMed Identifier
30996619
Citation
Halub ME, Spilman SK, Gaunt KA, Lamb KD, Jackson JA, Oetting TW, Sahr SM. High-flow nasal cannula therapy for patients with blunt thoracic injury: A retrospective study. Can J Respir Ther. 2016 Fall;52(4):110-113. Epub 2016 Nov 1.
Results Reference
result
PubMed Identifier
26060320
Citation
Gaunt KA, Spilman SK, Halub ME, Jackson JA, Lamb KD, Sahr SM. High-Flow Nasal Cannula in a Mixed Adult ICU. Respir Care. 2015 Oct;60(10):1383-9. doi: 10.4187/respcare.04016. Epub 2015 Jun 9.
Results Reference
result
PubMed Identifier
29208754
Citation
Lamb KD, Spilman SK, Oetting TW, Jackson JA, Trump MW, Sahr SM. Proactive Use of High-Flow Nasal Cannula With Critically Ill Subjects. Respir Care. 2018 Mar;63(3):259-266. doi: 10.4187/respcare.05793. Epub 2017 Dec 5.
Results Reference
result

Learn more about this trial

High Flow Nasal Cannula With Noninvasive Ventilation

We'll reach out to this number within 24 hrs