Point-of-Care Bedside Lung Ultrasound Examination Advanced Trial Protocol

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.

Conditions

• Acute Respiratory Distress Syndrome

Interventions

DEVICE

Linear Ultrasonic Sounder

Lung ultrasound evaluation is performed after clinical assessment and before chest radiography

DEVICE

Bedside X-ray Machine

Chest Radiography is performed after clinical evaluation without using ultrasound assessment.

Sponsors & Collaborators

• The second affiliated hospital of Jinan University School of Medicine

  collaborator UNKNOWN

• First Affiliated Hospital of Chengdu Medical College

  collaborator OTHER

• The First Affiliated Hospital with Nanjing Medical University

  collaborator OTHER

• Women and Children Health Hospital of Jiangsu Province

  collaborator UNKNOWN

• Affiliated Hospital of Sichuan Vocational College of Health and Rehabilitation

  collaborator UNKNOWN

• First Affiliated Hospital of Jinan University

  collaborator OTHER

• Yangzhou University

  collaborator OTHER

• The Third Affiliated Hospital of Southern Medical University

  collaborator OTHER_GOV

• The Sichuan Second Hospital of Guangxi Medical University

  collaborator UNKNOWN

• Guangzhou General Hospital

  collaborator OTHER

• Nankai University School of Medicine

  collaborator OTHER

• Guangdong Medical College

  collaborator OTHER

• Chongqing Medical University

  collaborator OTHER

• Tsinghua University

  collaborator OTHER

• Guiyang Medical University

  collaborator OTHER

• Shenzhen Institutes of Advanced Technology Chinese Academy of Science

  collaborator UNKNOWN

• Jiamusi University

  collaborator UNKNOWN

• The University of Science and Technology of China

  collaborator OTHER

• Nanjing Medical University

  lead OTHER

Principal Investigators

• Jie Zhou, MD · The First Affiliated Hospital with Nanjing Medical University

Study Design

Allocation

RANDOMIZED

Purpose

DIAGNOSTIC

Masking

DOUBLE

Model

PARALLEL

Eligibility

Min Age

1 Day

Max Age

31 Days

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2014-03-31

Primary Completion

2015-03-31

Completion

2015-03-31