Point of Care Ultrasound Lung Artificial Intelligence (AI) Validation Data Collection Study

Philips

Status: Completed

Conditions: Pleural Effusion; Lung Consolidation

Treatments: Device: Lung Ultrasound Scan

Study type: Observational

Funder types: Industry

Identifiers

NCT04891705

US-Lung AI-11237

Details and patient eligibility

About

This study is being conducted to collect image data and relevant clinical data from medical records of patients with suspicion of lung consolidation or pleural effusion. The information will be used to test the performance of Artificial Intelligence (AI) in identification of features associated with the above lung conditions.

Full description

This is a prospective, observational, multi-center, post-market clinical study. Enrollment will continue (up to a maximum of 500 adult subjects and up to 300 pediatric subjects) until diagnostic LUS exams are acquired for each of the following groups:

Approximately 500 Adult subjects targeting:

• Approximately 175 exams from patients positive for lung consolidation
• Approximately 175 exams from patients positive for pleural effusion
• Approximately 150 exams from patients negative for both conditions

Approximately 300 pediatric subjects targeting:

• Approximately 150 exams from patients positive for lung consolidation
• Approximately 150 exams from patients negative for lung consolidation

Enrollment: 554 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Subjects presenting to the Emergency Department, admitted to the hospital, or seen in the outpatient setting with suspicion of pleural effusion or lung consolidation who received chest imaging to include chest X-ray or CT, or for whom chest X-ray or CT are planned.

   Suspicion of pleural effusion or lung consolidation may be based upon imaging findings or presentation of symptoms including (but not limited to) dyspnea, hypoxia, tachypnea, rales, or dullness.

2. All attempts should be made for subjects to undergo scanning of 14 lung zones (adults) and 12 lung zones (pediatrics). Attempts should also be made to capture all required lung zones in adults and pediatrics. Instances where all zones cannot be captured need to be documented and reason for inability to scan them provided in EDC. See Section 8.1.3 Lung Ultrasound Exams.

3. Subject is willing to provide informed consent (or assent where age appropriate) to participate in the study. Subjects under 18 years of age require informed consent of a parent or guardian and assent as required by institutional IRB.

4. Weight of subject is greater than or equal to 10 kg.

Exclusion criteria

1. Subject has pathology precluding safe and pain-free ultrasound probe placement such as burn, significant soft tissue injury or surgical incisions.
2. Current imprisonment.
3. Pregnancy (self-reported)
4. Subjects with breast implants
5. Prior pleurodesis procedure.
6. History of severe lung disease and home oxygen use
7. Presence of subcutaneous air that precludes imaging
8. Body Mass Index (BMI) > 40
9. Significant scoliosis (Cobb angle ≥ 20 degrees).
10. Pediatric subjects with chronic lung diseases other than asthma.
11. Pediatric subjects on chronic respiratory support (i.e., nasal canula, CPAP, BiPAP, or tracheostomy).

Trial design

554 participants in 2 patient groups

Pleural Effusion

Description:

Adult and pediatric subjects with suspicion of pleural effusion

Treatment:

Device: Lung Ultrasound Scan

Lung Consolidation

Description:

Adult and pediatric subjects with suspicion of lung consolidation

Treatment:

Device: Lung Ultrasound Scan