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Effectiveness of Bronchodilator Nebulization With and Without Noninvasive Ventilation in COPD

Primary Purpose

Chronic Obstructive Pulmonary Disease (COPD), Type 2 Respiratory Failure

Status
Terminated
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
In-line nebulization through NIV mask
Off-NIV nebulization
Sponsored by
National University Health System, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease (COPD) focused on measuring Chronic Obstructive Pulmonary Disease (COPD), Nebulization, Respiratory failure, Non-invasive ventilation(NIV)

Eligibility Criteria

21 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥21 years.
  2. Known or suspected COPD (defined by a ratio of Forced Expiratory Volume in 1 second (FEV1) to Forced Vital Capacity (FVC) of less than 0.7).
  3. Acute decompensated type 2 respiratory failure (ABG pH ≤ 7.35 and PaCO2>45mmHg).
  4. Clinical decision made to start NIV.

Exclusion Criteria:

  1. Other acute decompensated type 2 respiratory failure related conditions (e.g. neuromuscular, heart failure etc.).
  2. Pneumonia present in the chest radiograph.
  3. Other conditions which may change lung impedance (e.g. heart failure or lung fibrosis).

Sites / Locations

  • National University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

In-line nebulization through NIV mask

Off-NIV nebulization

Arm Description

Bronchodilator nebulization is given through NIV circuit.

Bronchodilator nebulization is given during which NIV mask is taken off for a short time and reapplied when nebulization is finished.

Outcomes

Primary Outcome Measures

Difference in mean end-expiratory lung volumes between the two nebulization methods.
End-expiratory lung volumes between in-line nebulization and off-NIV nebulization.

Secondary Outcome Measures

Thickness of the diaphragm (by ultrasound) between in-line nebulization and off-NIV nebulization.
Measure thickness of the diaphragm between inspiration and expiration.
Changes in arterial blood gases in terms of pH and carbon dioxide between in-line. nebulization and off-NIV nebulization.
Measure changes of arterial blood gases between in-line nebulization and off-NIV. nebulization. Differences in pH (absolute,no unit) and carbon dioxide (in mmHg) will be noted.

Full Information

First Posted
March 15, 2018
Last Updated
October 10, 2022
Sponsor
National University Health System, Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT03481543
Brief Title
Effectiveness of Bronchodilator Nebulization With and Without Noninvasive Ventilation in COPD
Official Title
Effectiveness of Bronchodilator Nebulization With and Without Noninvasive Ventilation During Respiratory Failure in Chronic Obstructive Pulmonary Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment
Study Start Date
April 10, 2018 (Actual)
Primary Completion Date
November 12, 2020 (Actual)
Study Completion Date
November 12, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National University Health System, Singapore

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
The study aim to evaluate effectiveness of two bronchodilator nebulization strategies in patients with acute decompensated type 2 respiratory failure due to acute exacerbation of chronic obstructive pulmonary disease..
Detailed Description
Decompensated type 2 respiratory failure during acute exacerbation of chronic obstructive pulmonary disease (COPD) is treated with non-invasive ventilation (NIV) and nebulized bronchodilators. Nebulization during NIV can be applied by two methods: in-line nebulization through NIV mask and off-NIV nebulization during which NIV mask is taken off for a short time and reapplied when nebulization is finished. This study is a prospective randomized controlled trial to compare in-line nebulization through NIV versus off- NIV nebulization. After starting NIV in eligible COPD patients with type 2 respiratory failure, the baseline end-expiratory lung impedance (EELI) will be measured. Patient is randomized to receive either in-line or off-NIV nebulization. EELI will be measured again following completion of the nebulization, 15min after NIV is restarted (off-NIV group) or continued (in-line group). Ultrasound measurement of the thickness of the diaphragm will be recorded at baseline, 15min after NIV is restarted (off-NIV group) or continued (in-line group) and 48 hours after stopping the NIV. The main outcome measure, difference in mean end expiratory lung volume at 15min after NIV is restarted (off-NIV group) or continued (in-line group) between the two nebulization methods will be compared using independent sample T test. Thickness of the diaphragm and changes in the arterial blood gases (in terms of pH and carbon-di-oxide) will be compared between in-line nebulization and off-NIV nebulization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease (COPD), Type 2 Respiratory Failure
Keywords
Chronic Obstructive Pulmonary Disease (COPD), Nebulization, Respiratory failure, Non-invasive ventilation(NIV)

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
In-line nebulization through NIV mask
Arm Type
Experimental
Arm Description
Bronchodilator nebulization is given through NIV circuit.
Arm Title
Off-NIV nebulization
Arm Type
Active Comparator
Arm Description
Bronchodilator nebulization is given during which NIV mask is taken off for a short time and reapplied when nebulization is finished.
Intervention Type
Procedure
Intervention Name(s)
In-line nebulization through NIV mask
Intervention Description
In-line nebulization will be given through NIV circuit.
Intervention Type
Procedure
Intervention Name(s)
Off-NIV nebulization
Intervention Description
Bronchodilator nebulization is given during which NIV mask is taken off for a short time and reapplied when nebulization is finished..
Primary Outcome Measure Information:
Title
Difference in mean end-expiratory lung volumes between the two nebulization methods.
Description
End-expiratory lung volumes between in-line nebulization and off-NIV nebulization.
Time Frame
At baseline (approximately 15min after starting NIV) to approximately 15min after restarting (or continuing NIV) following the nebulization.
Secondary Outcome Measure Information:
Title
Thickness of the diaphragm (by ultrasound) between in-line nebulization and off-NIV nebulization.
Description
Measure thickness of the diaphragm between inspiration and expiration.
Time Frame
At baseline (approximately 15min after starting NIV) to approximately 15min after restarting (or continuing NIV) following the nebulization and repeated 48hours after stopping NIV.
Title
Changes in arterial blood gases in terms of pH and carbon dioxide between in-line. nebulization and off-NIV nebulization.
Description
Measure changes of arterial blood gases between in-line nebulization and off-NIV. nebulization. Differences in pH (absolute,no unit) and carbon dioxide (in mmHg) will be noted.
Time Frame
At baseline (approximately 15min after starting NIV) to approximately 15min after restarting (or continuing NIV) following the nebulization.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥21 years. Known or suspected COPD (defined by a ratio of Forced Expiratory Volume in 1 second (FEV1) to Forced Vital Capacity (FVC) of less than 0.7). Acute decompensated type 2 respiratory failure (ABG pH ≤ 7.35 and PaCO2>45mmHg). Clinical decision made to start NIV. Exclusion Criteria: Other acute decompensated type 2 respiratory failure related conditions (e.g. neuromuscular, heart failure etc.). Pneumonia present in the chest radiograph. Other conditions which may change lung impedance (e.g. heart failure or lung fibrosis).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amartya Mukhopadhyay, MBBS
Organizational Affiliation
National University Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
National University Hospital
City
Singapore
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
7651472
Citation
Brochard L, Mancebo J, Wysocki M, Lofaso F, Conti G, Rauss A, Simonneau G, Benito S, Gasparetto A, Lemaire F, et al. Noninvasive ventilation for acute exacerbations of chronic obstructive pulmonary disease. N Engl J Med. 1995 Sep 28;333(13):817-22. doi: 10.1056/NEJM199509283331301.
Results Reference
result
PubMed Identifier
22476448
Citation
Vivier E, Mekontso Dessap A, Dimassi S, Vargas F, Lyazidi A, Thille AW, Brochard L. Diaphragm ultrasonography to estimate the work of breathing during non-invasive ventilation. Intensive Care Med. 2012 May;38(5):796-803. doi: 10.1007/s00134-012-2547-7. Epub 2012 Apr 5.
Results Reference
result
PubMed Identifier
11316667
Citation
Pauwels RA, Buist AS, Calverley PM, Jenkins CR, Hurd SS; GOLD Scientific Committee. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease. NHLBI/WHO Global Initiative for Chronic Obstructive Lung Disease (GOLD) Workshop summary. Am J Respir Crit Care Med. 2001 Apr;163(5):1256-76. doi: 10.1164/ajrccm.163.5.2101039. No abstract available.
Results Reference
result

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Effectiveness of Bronchodilator Nebulization With and Without Noninvasive Ventilation in COPD

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