- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02636985
Application of Ultrasonic Elastography in Lung Lesions
Transthoracic Ultrasound Elastography in Pulmonary Lesions and Diseases
Elastography is an imaging of tissue elasticity or stiffness and is currently emerging as a mainstream tool for ultrasound-based diagnosis. This compressibility property of materials, mathematically expressed as the change in tissue displacement as a function of its distance from the compressing device, is known as strain and is the parameter that is imaged in an elastogram.
Elastography has currently shown promising result in differentiating viscoelastic nature of various organs, which is a consequence of certain underlying diseases.
At present, there are limited literatures revealing the application and feasibility of ultrasonic elastography in lung lesions. This is essentially important as it may serve as an adjuvant to B-mode ultrasound. The investigators aimed at exploring the application and feasibility of ultrasonic elastography on lung lesions.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Taipei City
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Taipei, Taipei City, Taiwan, 100
- National Taiwan University Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
A. Inclusion Criteria:
Patients with radiographic findings of:
- consolidation
- obstructive pneumonitis
- tumors
B. Exclusion Criteria:
- Patients with poor acoustic window
- Unable to hold breathing
- Not cooperative
- Presence of pleural effusion
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of strain ratio between necrosis, atelectasis, consolidation and tumor
Time Frame: Up to 15 months
|
The strain ratio was measured under ultrasonic elastography.
At least three measurements were performed each time and we average all the measurements as the final strain ratio.
Independent t test was used for comparison.
|
Up to 15 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Hao-Chien Wang, MD, PhD, National Taiwan University Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 201503075RINC
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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