Measurements and Characterization of Doppler Signals From the Right Chest in Pediatric and Adult Patients
Evaluation of Lung Doppler Signals in Pediatric and Adult Patients
1 other identifier
observational
230
1 country
2
Brief Summary
Recently it has been shown that clear reproducible Doppler signals can be recorded from the lung parenchyma by means of a pulsed Doppler ultrasound system incorporating a special signal processing package parametric Doppler, TPD, EchoSense Ltd., Haifa, Israel). These lung Doppler signals (LDS) are in full synchrony with the cardiac cycle and can be obtained from the lungs, including areas remote from the heart and main pulmonary vessels. The LDS waves typically have peak velocities of up to 30 cm/s and are of relatively high power, making it possible to detect them despite the aforementioned attenuation by the air in the lungs. The LDS are thought to represent the radial wall movement of small pulmonary blood vessels, caused by pressure pulse waves of cardiac origin which propagate throughout the lung vasculature. The LDS may contain information of significant diagnostic and physiological value regarding the pulmonary parenchyma and vasculature, as well as the cardio-vascular system in general. Pulmonary arterial hypertension (PAH) is a condition characterized by reshaping of the small pulmonary arteries with increase in pulmonary vascular resistance, leading gradually to right-sided cardiac failure. A trans-thoracic echocardiograph (TTE) is a test classically undertaken in order to screen for pulmonary hypertension. However, the systolic pulmonary artery pressure (SPAP) values thereby obtained are often imprecise and depend upon the expertise of the individual carrying out the test. Therefore, the pulmonary arterial pressure and cardiac output values have to be ascertained with a right-sided cardiac catheterization, which is considered the gold-standard, but is invasive. In a pilot study of adult PAH patients (unpublished), lung Doppler signals have been shown to have the potential to diagnose pulmonary hypertension in two different ways: First, by measuring the degree of attenuation of the LDS during acute pressure rise in the chest cavity (i.e. during Valsalva maneuver). Second, by detecting differences between the LDS in patients with PAH and control subjects. One of the objectives of the present study is to evaluate the lung Doppler signals in pediatric patients of various age groups, with and without pulmonary vascular disease. The second objective of the study is to verify previous findings of abnormal lung Doppler signals in adult patients with pulmonary hypertension.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2013
Longer than P75 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2013
CompletedFirst Submitted
Initial submission to the registry
July 25, 2013
CompletedFirst Posted
Study publicly available on registry
August 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2021
CompletedMarch 23, 2022
June 1, 2019
8 years
July 25, 2013
March 22, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Diagnose specific pattern of LDS in children by features as velocity & power in comparison to adult LDS pattern.
1 year to collect all data and obtain an average diagnostic pattern
Study Arms (3)
Adults w/ PH
Subjects above 18y scheduled to undergo RHC for Doppler ultrasound external right chest wall tests
Children w/ PH
Children 0-18y old scheduled to RHC
Children control
Children 0-18y old w/o PH for Lung Doppler tests as controls
Interventions
Doppler Ultrasound recording on external right chest wall
Eligibility Criteria
The study targets to enroll 200 patients (see inclusion criteria): 100 patients will be children without cardiopulmonary diseases, 50 patients will be children undergoing heart catheterization, 50 patients will be adults undergoing heart catheterization
You may qualify if:
- Adults undergoing RHC:
- Males or females aged over 18 years
- With suspicion or diagnosis of pulmonary hypertension.
- Scheduled to undergo right heart catheterization
- Able and willing to give informed consent
- Pediatric patients undergoing RHC:
- Males or females aged 0-18 years
- Scheduled to undergo right hear catheterization
- Parents willing to give informed consent
- Pediatric patients without significant cardio-pulmonary diseases:
- Males or females aged 0-18 years Not known to have a significant cardiac or pulmonary disease
- Legal guardians willing to give informed consent
You may not qualify if:
- Hemodynamically unstable patients.
- For adult and pediatric patients undergoing right heart catheterization:
- a. Any contra-indication to perform the procedure
- For adults only:
- Patients incapable of performing a Valsalva maneuver
- Patients with recent (within the past 3 months) myocardial infarction, high degree AV block, severe aortic stenosis or open angle glaucoma
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Echosense Ltd.lead
Study Sites (2)
Stanford Hospital and Clinics and Lucile Packard Children's Hospital
Palo Alto, California, United States
Stanford university hospital
Palo Alto, California, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jeffery Feinstein, MD
Stanford Hospital and Clinics and Lucile Packard Children's Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 25, 2013
First Posted
August 1, 2013
Study Start
July 1, 2013
Primary Completion
July 1, 2021
Study Completion
July 1, 2021
Last Updated
March 23, 2022
Record last verified: 2019-06