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| Name | Class |
|---|---|
| Rhode Island Hospital | OTHER |
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The purpose of this study is to compare the Total Face Maskâ„¢ (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).
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 â„¢ (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 â„¢ 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 â„¢ 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 â„¢ 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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Patients receiving NPPV by the 'Total Face Mask' |
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| 2 | Active Comparator | Patients receiving NPPV by 'standard oronasal mask' |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Total face mask (interface for NPPV) | Device | NPPV is applied by this mask, as long as NPPV is received. |
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| Measure | Description | Time Frame |
|---|---|---|
| Mask Comfort (as Determined by the Visual Analog Scores 1 Being Least, 10 Being Most) | During the first 3 hours of recruitment | |
| Time Required for Mask Placement | at the initiation of NPPV |
| Measure | Description | Time Frame |
|---|---|---|
| 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 | During hospitalization period (after recruitment into the study) |
| Deterioration Vital Signs |
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Inclusion Criteria:
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:
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| Name | Affiliation | Role |
|---|---|---|
| Aylin Ozsancak, MD | Research Fellow | Study Chair |
| Nicholas S. Hill, MD | Chair of Pulmonary, Critical Care and Sleep Division | Principal Investigator |
| Samy Sidhom, MD, MPH | Clinical Fellow | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Tufts Medical Center | Boston | Massachusetts | 02111 | United States | ||
| Rhode Island Hospital |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 21330385 | Result | 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. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Total Face Mask | Patients receiving NPPV by the 'Total Face Mask' or standard face mask controls |
| FG001 | Standard Face Mask Controls | Patients receiving NPPV by 'standard oronasal mask' |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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| ID | Title | Description |
|---|---|---|
| BG000 | Total Face Mask | Patients receiving NPPV by the 'Total Face Mask' or standard face mask controls |
| BG001 | Standard Face Mask Controls | Patients receiving NPPV by 'standard oronasal mask' |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Mask Comfort (as Determined by the Visual Analog Scores 1 Being Least, 10 Being Most) | By power analysis | Posted | Mean | Standard Error | units on a scale | During the first 3 hours of recruitment |
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Total Face Mask | Patients receiving NPPV by the 'Total Face Mask' or standard face mask controls |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Claustrophobia | Respiratory, thoracic and mediastinal disorders | Claustrophobia in 4 control patients and 6 Total Face mask patients |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Nicholas Hill MD | Tufts Medical Center | 617-636-4288 | nhill@tuftsmedicalcenter.org |
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| Comfort full or RT040 oronasal mask (interface for NPPV) | Device | 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. |
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| during the first 24 hours of the study |
| Deterioration in Gas Exchange | during the first 24 hours of the study |
| Total Length of Time Requiring NIV | during hospitalization (after recruitment) |
| Length of Hospital Stay | during hospitalization (after recruitment) |
| In-hospital Mortality Rate | during hospitalization (after recruitment) |
| Providence |
| Rhode Island |
| 02903 |
| United States |
| BG002 | Total | Total of all reporting groups |
| years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| Primary | Time Required for Mask Placement | Posted | Median | Inter-Quartile Range | Minutes | at the initiation of NPPV |
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| Secondary | 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 | Posted | Count of Participants | Participants | During hospitalization period (after recruitment into the study) |
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| Secondary | Deterioration Vital Signs | Posted | Count of Participants | Participants | during the first 24 hours of the study |
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| Secondary | Deterioration in Gas Exchange | Posted | Count of Participants | Participants | during the first 24 hours of the study |
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| Secondary | Total Length of Time Requiring NIV | Posted | Median | Inter-Quartile Range | Hours | during hospitalization (after recruitment) |
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| Secondary | Length of Hospital Stay | Posted | Mean | Full Range | Days | during hospitalization (after recruitment) |
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| Secondary | In-hospital Mortality Rate | Posted | Count of Participants | Participants | during hospitalization (after recruitment) |
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| 0 |
| 29 |
| 6 |
| 29 |
| EG001 | Standard Face Mask Controls | Patients receiving NPPV by 'standard oronasal mask' | 0 | 31 | 4 | 31 |
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