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Diagnosis of Cardio-Pulmonary Pathology Using Transthoracic Parametric Doppler (TPD)

Detection and Characterization of Cardio-Pulmonary Patho-Physiological States and Diseases by Transthoracic Parametric Doppler (TPD)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01361139
Enrollment
500
Registered
2011-05-26
Start date
2011-08-31
Completion date
2014-11-30
Last updated
2015-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, Hypertension, Pulmonary, Lung Disease, Chronic Obstructive, Lung Disease, Interstitial, Sarcoidosis

Keywords

Chronic obstructive lung disease, Interstitial lung disease, Asthma, Sarcoidosis, Pulmonary hypertension, Ultrasound, Doppler, Lung disease diagnosis

Brief summary

This is a study that seeks to characterize data obtained from patients with a variety of lung diseases using ultrasound signals obtained from the lung tissue. A standard ultrasound instrument in the doppler mode (not the imaging mode used in examination of pregnant women for instance) is placed on the chest wall and the unique software the investigators have developed analyzes the signal reflected back from within the lung. On the basis of pilot studies performed previously the investigators expect to receive different signals from different diseases. The investigators seek to further characterize these signals to enable accurate diagnosis of different lung diseases using our technology.

Interventions

None listed

Sponsors

Clalit Health Services, Haifa and West Galilee
CollaboratorOTHER
Echosense Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Age 18 years or older Patients who are clinically suspected of having pulmonary, cardiac or Cardio-pulmonary disease preferably any one or more of the conditions listed below: * Patients with CHF * Patients with pulmonary hypertension with documented right heart catheterization data * Patients with COPD in two subgroups: * Emphysema, (evidence of emphysema on High Resolution Computed Tomography, (HRCT) and airflow limitation of GOLD II severity who have had Carbon Monoxide Diffusing capacity, (DLCO) and Residual Volume(RV) measured, or patients without HRCT with measurements of lung volumes and diffusing capacity with Total Lung Capacity (TLC) ≥1.0 predicted, RV/TLC ≥0.4, DLCO ≤ 0.7 predicted. * Chronic Bronchitis (No evidence of Emphysema on HRCT and/or no evidence of air-trapping or reduced DLCO.) * Patients with asthma according to ATS/ERS definition, * Patients with interstitial lung disease (ILD) of any etiology including sarcoidosis diagnosed by HRCT in sub groups as follows: * Mild ILD (TLC 0.71-0.79 predicted, DLCO ≥ 0.71 predicted) * Moderate and severe ILD (TLC ≤ 0.7 predicted, DLCO ≤ 0.7 predicted) * Signed informed consent. * Patients with sarcoidosis without evidence of parenchymal lung disease defined as normal DLCO and/or HRCT.

Exclusion criteria

* Patients unable to cooperate. * Inability to assume a semi-reclining or supine position * Patients with severe chest wall deformity

Design outcomes

Primary

MeasureTime frame
Diagnose specific pattern of the LDS signals as Power and Velocity in pulmonary diseases in comparison to controls.1 year

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026