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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02636985
Other study ID # 201503075RINC
Secondary ID
Status Completed
Phase N/A
First received November 24, 2015
Last updated December 17, 2015
Start date December 2011
Est. completion date March 2013

Study information

Verified date December 2015
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

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.


Description:

Patients performed conventional B-mode ultrasound, subsequently followed by ultrasound elastography. The strain ration was measured and was compared between necrosis, atelectasis, consolidation and tumor.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility A. Inclusion Criteria:

Patients with radiographic findings of:

1. consolidation

2. obstructive pneumonitis

3. tumors

B. Exclusion Criteria:

1. Patients with poor acoustic window

2. Unable to hold breathing

3. Not cooperative

4. Presence of pleural effusion

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei Taipei City

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of strain ratio between necrosis, atelectasis, consolidation and tumor 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 Yes
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