Point-of-Care Bedside Lung Ultrasound Examination Advanced Trial Protocol (PoCBLUEPlus)
Primary Purpose
Acute Respiratory Distress Syndrome
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Linear Ultrasonic Sounder
Bedside X-ray Machine
Sponsored by
About this trial
This is an interventional diagnostic trial for Acute Respiratory Distress Syndrome focused on measuring Acute Respiratory Distress Syndrome
Eligibility Criteria
Inclusion Criteria:
- All infants who present to the ICU with respiratory symptoms suspicious for ARDS, according to Pediatric Acute Respiratory Distress Syndrome: Consensus Recommendations From the Pediatric Acute Lung Injury Consensus Conference, which is proposed by The Pediatric Acute Lung Injury Consensus Conference Group.
- In whom the treating Collaborative Review Groups of Poc-BLUE-Plus protocol believe would benefit from diagnostic imaging.
Exclusion Criteria:
- Infants who arrive at the ICU with a previously performed chest radiography
- Unstable infants with life-threatening injuries who require ongoing resuscitation
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Lung Ultrasound
Chest Radiography
Arm Description
In infants allocated to this arm Lung ultrasound for detection of ARDS will be performed before chest radiography.
In infants allocated to this arm chest radiography will be performed for the detection of indirect signs of ARDS without ultrasound evaluation.
Outcomes
Primary Outcome Measures
Accuracy of Lung Ultrasound in Neonatal ARDS
Accuracy of lung ultrasound and chest radiography will be measured using as gold standard the independent evaluation of the entire medical records by two expert emergency physicians blinded to the lung ultrasound results and radiographic reports (digitalized chest radiography images will be available).
Secondary Outcome Measures
Accuracy of Lung Ultrasound in the Ventilator-Associated Pneumonia
Accuracy of lung ultrasound and chest radiography will be measured using as gold standard the independent evaluation of the entire medical records by two expert emergency physicians blinded to the lung ultrasound results and radiographic reports (digitalized chest radiography images will be available).
Accuracy of Lung Ultrasound in the Weaning of Ventilatory Support
Accuracy of lung ultrasound and chest radiography will be measured using as gold standard the independent evaluation of the entire medical records by two expert emergency physicians blinded to the lung ultrasound results and radiographic reports (digitalized chest radiography images will be available).
Full Information
NCT ID
NCT02403791
First Posted
March 22, 2015
Last Updated
March 25, 2015
Sponsor
Nanjing Medical University
Collaborators
The second affiliated hospital of Jinan University School of Medicine, First Affiliated Hospital of Chengdu Medical College, The First Affiliated Hospital with Nanjing Medical University, Women and Children Health Hospital of Jiangsu Province, Affiliated Hospital of Sichuan Vocational College of Health and Rehabilitation, First Affiliated Hospital of Jinan University, Yangzhou University, The Third Affiliated Hospital of Southern Medical University, The Sichuan Second Hospital of Guangxi Medical University, Guangzhou General Hospital, Nankai University School of Medicine, Guangdong Medical College, Chongqing Medical University, Tsinghua University, Guiyang Medical University, Shenzhen Institutes of Advanced Technology Chinese Academy of Science, Jiamusi University, The University of Science and Technology of China
1. Study Identification
Unique Protocol Identification Number
NCT02403791
Brief Title
Point-of-Care Bedside Lung Ultrasound Examination Advanced Trial Protocol
Acronym
PoCBLUEPlus
Official Title
A Prospective, Multi-center, Open-label and Double-blind, Standard-controlled, Non-inferiority, Diagnostic Study of Lung Ultrasound for Management of Mechanical Ventilation in Neonatal Acute Respiratory Distress Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nanjing Medical University
Collaborators
The second affiliated hospital of Jinan University School of Medicine, First Affiliated Hospital of Chengdu Medical College, The First Affiliated Hospital with Nanjing Medical University, Women and Children Health Hospital of Jiangsu Province, Affiliated Hospital of Sichuan Vocational College of Health and Rehabilitation, First Affiliated Hospital of Jinan University, Yangzhou University, The Third Affiliated Hospital of Southern Medical University, The Sichuan Second Hospital of Guangxi Medical University, Guangzhou General Hospital, Nankai University School of Medicine, Guangdong Medical College, Chongqing Medical University, Tsinghua University, Guiyang Medical University, Shenzhen Institutes of Advanced Technology Chinese Academy of Science, Jiamusi University, The University of Science and Technology of China
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study was to evaluate the availability and diagnostic accuracy of point-of-care bedside lung ultrasound examination in management of mechanical ventilation in neonatal acute respiratory distress syndrome.
Detailed Description
Neonatal acute respiratory distress syndrome (ARDS) is a critical condition requiring dynamic evaluation and interventions. Point-of-care bedside lung ultrasound examination (PoC-BLUE) is a noninvasive, readily available imaging modality that can complement physical and clinical evaluation.
At any time, most neonates and infants with ARDS in medical intensive care units (ICUs) require mechanical ventilation, making it one of the most frequently used critical care technologies. However, difficulties with regard to the accurate diagnosis of ARDS before administration of mechanical ventilation, dynamic monitoring of treatment effects during administration of mechanical ventilation, and decision-making of timing in weaning from mechanical ventilation, are often encountered in the majority neonates and infants who require mechanical ventilation.
Hence, techniques that expedite and advance the knowledge of the administration of mechanical ventilation should have an important clinical significance in the diagnosis, treatment and prognosis of ARDS.
Preliminary researches have suggested that BLUE has a high diagnostic accuracy in patients with acute respiratory failure, and has the potential to quantify the rate and degree of diaphragm thinning during mechanical ventilation, which may be useful to predict extubation success or failure during either spontaneous breathing (SB) or pressure support (PS) trials.
Unfortunately, few studies focus on the availability of PoC-BLUE in management of mechanical ventilation in neonatal acute respiratory distress syndrome. Also, they call into question the possible association of the demographic and clinical confounders with the diagnostic accuracy of PoC-BLUE for diagnosis, monitoring and prognosis of ARDS in the whole process of mechanical ventilation.
Given that a considerable need for a timely and dynamic diagnosis of severe condition and therapy evaluation during mechanical ventilation has been triggered to integrate the currently available bulk of knowledge and information, the objective of this study is to investigate the availability and diagnostic accuracy of PoC-BLUE Plus protocol in management of mechanical ventilation in ARDS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome
Keywords
Acute Respiratory Distress Syndrome
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1000 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lung Ultrasound
Arm Type
Experimental
Arm Description
In infants allocated to this arm Lung ultrasound for detection of ARDS will be performed before chest radiography.
Arm Title
Chest Radiography
Arm Type
Active Comparator
Arm Description
In infants allocated to this arm chest radiography will be performed for the detection of indirect signs of ARDS without ultrasound evaluation.
Intervention Type
Device
Intervention Name(s)
Linear Ultrasonic Sounder
Other Intervention Name(s)
Bedside Ultrasonography System
Intervention Description
Lung ultrasound evaluation is performed after clinical assessment and before chest radiography
Intervention Type
Device
Intervention Name(s)
Bedside X-ray Machine
Other Intervention Name(s)
Chest X-ray System
Intervention Description
Chest Radiography is performed after clinical evaluation without using ultrasound assessment.
Primary Outcome Measure Information:
Title
Accuracy of Lung Ultrasound in Neonatal ARDS
Description
Accuracy of lung ultrasound and chest radiography will be measured using as gold standard the independent evaluation of the entire medical records by two expert emergency physicians blinded to the lung ultrasound results and radiographic reports (digitalized chest radiography images will be available).
Time Frame
Accuracy will be measured at the end of clinical evaluation in the ICU, an expected average of 4 days
Secondary Outcome Measure Information:
Title
Accuracy of Lung Ultrasound in the Ventilator-Associated Pneumonia
Description
Accuracy of lung ultrasound and chest radiography will be measured using as gold standard the independent evaluation of the entire medical records by two expert emergency physicians blinded to the lung ultrasound results and radiographic reports (digitalized chest radiography images will be available).
Time Frame
Accuracy will be measured at the end of clinical evaluation in the ICU, an expected average of 4 days
Title
Accuracy of Lung Ultrasound in the Weaning of Ventilatory Support
Description
Accuracy of lung ultrasound and chest radiography will be measured using as gold standard the independent evaluation of the entire medical records by two expert emergency physicians blinded to the lung ultrasound results and radiographic reports (digitalized chest radiography images will be available).
Time Frame
Accuracy will be measured at the end of clinical evaluation in the ICU, an expected average of 4 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
31 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All infants who present to the ICU with respiratory symptoms suspicious for ARDS, according to Pediatric Acute Respiratory Distress Syndrome: Consensus Recommendations From the Pediatric Acute Lung Injury Consensus Conference, which is proposed by The Pediatric Acute Lung Injury Consensus Conference Group.
In whom the treating Collaborative Review Groups of Poc-BLUE-Plus protocol believe would benefit from diagnostic imaging.
Exclusion Criteria:
Infants who arrive at the ICU with a previously performed chest radiography
Unstable infants with life-threatening injuries who require ongoing resuscitation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jie Zhou, MD
Organizational Affiliation
The First Affiliated Hospital with Nanjing Medical University
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
25647235
Citation
Pediatric Acute Lung Injury Consensus Conference Group. Pediatric acute respiratory distress syndrome: consensus recommendations from the Pediatric Acute Lung Injury Consensus Conference. Pediatr Crit Care Med. 2015 Jun;16(5):428-39. doi: 10.1097/PCC.0000000000000350.
Results Reference
result
PubMed Identifier
18359431
Citation
Muscedere J, Dodek P, Keenan S, Fowler R, Cook D, Heyland D; VAP Guidelines Committee and the Canadian Critical Care Trials Group. Comprehensive evidence-based clinical practice guidelines for ventilator-associated pneumonia: diagnosis and treatment. J Crit Care. 2008 Mar;23(1):138-47. doi: 10.1016/j.jcrc.2007.12.008.
Results Reference
result
PubMed Identifier
22797452
Citation
ARDS Definition Task Force; Ranieri VM, Rubenfeld GD, Thompson BT, Ferguson ND, Caldwell E, Fan E, Camporota L, Slutsky AS. Acute respiratory distress syndrome: the Berlin Definition. JAMA. 2012 Jun 20;307(23):2526-33. doi: 10.1001/jama.2012.5669.
Results Reference
result
PubMed Identifier
11742959
Citation
MacIntyre NR, Cook DJ, Ely EW Jr, Epstein SK, Fink JB, Heffner JE, Hess D, Hubmayer RD, Scheinhorn DJ; American College of Chest Physicians; American Association for Respiratory Care; American College of Critical Care Medicine. Evidence-based guidelines for weaning and discontinuing ventilatory support: a collective task force facilitated by the American College of Chest Physicians; the American Association for Respiratory Care; and the American College of Critical Care Medicine. Chest. 2001 Dec;120(6 Suppl):375S-95S. doi: 10.1378/chest.120.6_suppl.375s. No abstract available.
Results Reference
result
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Point-of-Care Bedside Lung Ultrasound Examination Advanced Trial Protocol
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