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Evaluation Of The Total Face Mask For Emergency Application In Acute Respiratory Failure

Primary Purpose

Acute Respiratory Insufficiency

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Total face mask (interface for NPPV)
Comfort full or RT040 oronasal mask (interface for NPPV)
Sponsored by
Tufts Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Insufficiency focused on measuring acute respiratory insufficiency, noninvasive ventilation, oronasal face mask, total face mask

Eligibility Criteria

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

Inclusion Criteria:

  • Age>18
  • Either A or B

A. Clinical Criteria: Moderate to severe respiratory distress as evidenced by tachypnea, use of accessory muscles for breathing, or abdominal paradox.

B. Blood Gas and Physiologic Criteria: Gas exchange abnormalities including PaCO2>45 with a pH<7.35, or a PaO2/FiO2 ratio<200.

Exclusion Criteria:

  • The need for immediate intubation
  • Medical instability such as hypotensive shock, uncontrolled cardiac ischemia or arrythmias, unstable myocardial infarction, uncontrolled upper gastrointestinal bleeding
  • Agitation or uncooperativeness, unresponsive to small doses of sedatives
  • Excretions or inability to protect the airway
  • Inability to fit the mask
  • Facial trauma
  • Upper airway obstruction

Sites / Locations

  • Tufts Medical Center
  • Rhode Island Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Patients receiving NPPV by the 'Total Face Mask'

Patients receiving NPPV by 'standard oronasal mask'

Outcomes

Primary Outcome Measures

Mask Comfort (as Determined by the Visual Analog Scores 1 Being Least, 10 Being Most)
Time Required for Mask Placement

Secondary Outcome Measures

Early NIV Discontinuation Rate
Defined as the inability of the patient to be maintained on NPPV using the assigned mask while there was still an indication for ventilatory support
Deterioration Vital Signs
Deterioration in Gas Exchange
Total Length of Time Requiring NIV
Length of Hospital Stay
In-hospital Mortality Rate

Full Information

First Posted
May 27, 2008
Last Updated
May 25, 2018
Sponsor
Tufts Medical Center
Collaborators
Rhode Island Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00686257
Brief Title
Evaluation Of The Total Face Mask For Emergency Application In Acute Respiratory Failure
Official Title
Evaluation Of The Total Face Mask For Emergency Application In Acute Respiratory Failure
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
January 2003 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tufts Medical Center
Collaborators
Rhode Island Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the Total Face Mask™ (Respironics, Inc., Pittsburgh, PA) (covering whole face) and the standard oronasal facemask (covering nose and mouth) for the emergency treatment of patients with acute respiratory failure with the machine blowing air into the mask placed on the face (noninvasive positive pressure ventilation) (NPPV).
Detailed Description
Despite its demonstrated efficacy in treating selected patients with acute respiratory failure, the application of NPPV is still plagued by a substantial failure rate, ranging from below 10% to above 40%. Mask intolerance ranks as one of the most common causes of failure. This is related to ill-fitting masks, mask discomfort (despite a properly fitted mask), excessively tightened straps, excessive air leaks around the mask or through the mouth, and claustrophobia. The most commonly used masks in the acute care setting are either oronasal masks that cover the nose and mouth, or nasal masks that cover the nose alone. Both mask types usually consist of clear plastic dome-shaped mask with a soft silicon gasket to create an air seal with the skin. While this approach is usually successful, it may lead to patient discomfort and/or an air leak secondary to the difficulty in creating an effective seal over the bridge of the nose and over mobile structures such as the mandible. The Total Face Mask ™ (Respironics, Inc., Pittsburgh, PA) uses a different approach to avoid some of these limitations. Considerably larger than a standard oronasal mask, it covers the entire face and creates an air seal using a silicon gasket around the parameter of the face. In this way, gasket pressure is more evenly distributed, and discomfort over the bridge of the nose or chin is eliminated, and air leaking reduced. In addition, because one mask size fits virtually all patients, the Total Face Mask ™ facilitates the fitting process and permits more rapid initiation of ventilatory assistance. Clinical experience to date suggests that claustrophobia is not a common problem with the Total Face Mask ™ despite its size, and that its contribution to dead space is comparable to that of most oronasal masks. The following protocol aims to compare use of the Total Face Mask ™ to the Comfort Full oronasal mask (also by Respironics, Inc., Pittsburgh, PA)or RT040 oronasal mask (Fisher&Paykel Inc., Wellington, NZ) in the acute care setting for patients meeting standard indications for NPPV.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Insufficiency
Keywords
acute respiratory insufficiency, noninvasive ventilation, oronasal face mask, total face mask

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Patients receiving NPPV by the 'Total Face Mask'
Arm Title
2
Arm Type
Active Comparator
Arm Description
Patients receiving NPPV by 'standard oronasal mask'
Intervention Type
Device
Intervention Name(s)
Total face mask (interface for NPPV)
Other Intervention Name(s)
cephalic mask
Intervention Description
NPPV is applied by this mask, as long as NPPV is received.
Intervention Type
Device
Intervention Name(s)
Comfort full or RT040 oronasal mask (interface for NPPV)
Other Intervention Name(s)
Full face mask
Intervention Description
NPPV is applied by one of these masks (Comfort full or RT040 masks used at Rhode Island Hospital and Tufts Medical Center respectively), as long as NPPV is received.
Primary Outcome Measure Information:
Title
Mask Comfort (as Determined by the Visual Analog Scores 1 Being Least, 10 Being Most)
Time Frame
During the first 3 hours of recruitment
Title
Time Required for Mask Placement
Time Frame
at the initiation of NPPV
Secondary Outcome Measure Information:
Title
Early NIV Discontinuation Rate
Description
Defined as the inability of the patient to be maintained on NPPV using the assigned mask while there was still an indication for ventilatory support
Time Frame
During hospitalization period (after recruitment into the study)
Title
Deterioration Vital Signs
Time Frame
during the first 24 hours of the study
Title
Deterioration in Gas Exchange
Time Frame
during the first 24 hours of the study
Title
Total Length of Time Requiring NIV
Time Frame
during hospitalization (after recruitment)
Title
Length of Hospital Stay
Time Frame
during hospitalization (after recruitment)
Title
In-hospital Mortality Rate
Time Frame
during hospitalization (after recruitment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age>18 Either A or B A. Clinical Criteria: Moderate to severe respiratory distress as evidenced by tachypnea, use of accessory muscles for breathing, or abdominal paradox. B. Blood Gas and Physiologic Criteria: Gas exchange abnormalities including PaCO2>45 with a pH<7.35, or a PaO2/FiO2 ratio<200. Exclusion Criteria: The need for immediate intubation Medical instability such as hypotensive shock, uncontrolled cardiac ischemia or arrythmias, unstable myocardial infarction, uncontrolled upper gastrointestinal bleeding Agitation or uncooperativeness, unresponsive to small doses of sedatives Excretions or inability to protect the airway Inability to fit the mask Facial trauma Upper airway obstruction
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aylin Ozsancak, MD
Organizational Affiliation
Research Fellow
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nicholas S. Hill, MD
Organizational Affiliation
Chair of Pulmonary, Critical Care and Sleep Division
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Samy Sidhom, MD, MPH
Organizational Affiliation
Clinical Fellow
Official's Role
Study Director
Facility Information:
Facility Name
Tufts Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
Rhode Island Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21330385
Citation
Ozsancak A, Sidhom SS, Liesching TN, Howard W, Hill NS. Evaluation of the total face mask for noninvasive ventilation to treat acute respiratory failure. Chest. 2011 May;139(5):1034-1041. doi: 10.1378/chest.10-1905. Epub 2011 Feb 17.
Results Reference
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Evaluation Of The Total Face Mask For Emergency Application In Acute Respiratory Failure

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