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Significance of Ultrasound Elastography in Lymph Node

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03391557
Recruitment Status : Unknown
Verified January 2018 by Fangsurong, Nanjing First Hospital, Nanjing Medical University.
Recruitment status was:  Active, not recruiting
First Posted : January 5, 2018
Last Update Posted : January 25, 2018
Sponsor:
Collaborator:
Johns Hopkins University
Information provided by (Responsible Party):
Fangsurong, Nanjing First Hospital, Nanjing Medical University

Brief Summary:
Background and Objectives: Elastography can reflect the difference of tissue hardness, which helps to identify the difference of hardness between benign and malignant tissues. The aim of this study was to evaluate the value of endobronchial ultrasound elastography in the differential diagnosis of benign and malignant intrathoracic lymph nodes. Materials and Methods: A total of 42 patients with intrathoracic lymphadenopathy required for EBUS-TBNA examination were prospectively enrolled. Firstly, All patients were evaluated by enhanced chest CT examination,the EBUS B-mode ultrasound and EBUS-guided elastography before EBUS-TBNA.Then, the investigators evaluated every lymph node by describing the characteristics of the CT image (Short diameter, texture, shape, boundary ,mean CT value), B-mode ultrasound (short diameter, echo characteristic, shape, boundary) and elastography (image type, grading score, strain rate, blue area ratio). Finally, the pathological results were used as the gold standard. the investigators compare the characteristics of the 3 evaluating methods alone and in combination between benign and malignant lymph nodes.

Condition or disease Intervention/treatment Phase
Lung Cancer Diagnostic Test: UE Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 42 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: Patients who underwent EBUS-TBNA examination in department of respiration,Nanjing Hospital Affiliated to Nanjing Medical University during 21June 2016 and 17 April 2017 were included in the study, All patients were evaluated by chest enhanced CT and/or 18-FDG PET-CT,those who had enlarged intrathoracic lymph nodes(≥1cm) and/or 18-FDG high uptake (SUV Max > 2.5) without bleeding tendency, abnormal coagulation function and serious cardiac dysfunction.
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Significance of Endoscopic Ultrasonography Guided Transbronchial Lymph Node Biopsy (TBNA) and Ultrasound Elastography in Lymph Node
Actual Study Start Date : June 21, 2016
Actual Primary Completion Date : April 17, 2017
Estimated Study Completion Date : December 31, 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Patients with the UE examination
Patients with enlarged intrathoracic lymph nodes(≥1cm) and/or 18-FDG high uptake (SUV Max > 2.5) without bleeding tendency, abnormal coagulation function and serious cardiac dysfunction were finally selected.
Diagnostic Test: UE
All patients were examined by enhanced chest computed tomography (CT), the B-mode ultrasound and endobronchial ultrasound (EBUS)guided elastography before EBUS-TBNA. Each lymph node was assessed by describing the characteristics of the CT image (short diameter, texture, shape, boundary, mean CT value), B-mode ultrasound (short diameter, echo characteristic, shape, boundary) and ultrasound elastography (image type, grading score, strain rate, blue area ratio).
Other Name: Ultrasound Elastography




Primary Outcome Measures :
  1. The echo characteristic of the B-mode ultrasound of lymph nodes. [ Time Frame: 10 minutes ]
    echo characteristic(hypoechoic or not hypoechoic, homogeneous or not)


Secondary Outcome Measures :
  1. The shape of the B-mode ultrasound of lymph nodes. [ Time Frame: 10 minutes ]
    shape (round or not)

  2. The boundary of the B-mode ultrasound of lymph nodes. [ Time Frame: 10 minutes ]
    boundary (clear or not)

  3. The short diameter of the B-mode ultrasound of lymph nodes. [ Time Frame: 10 minutes ]
    short diameter (millimeter,mm)

  4. The image type of the elastography of lymph nodes. [ Time Frame: 10 minutes ]
    image type ( Type 1: mainly non-blue (green and red);Type 2: partly blue, partly non-blue (green and red); Type 3: mainly blue )

  5. The strain ratio of the elastography of lymph nodes. [ Time Frame: 10 minutes ]
    strain ratio (ratio result)

  6. The blue area ratio of the elastography of lymph nodes. [ Time Frame: 15 minutes ]
    blue area ratio (The percentage of the number of blue pixels in the total number of pixels of the entire lymph node image,%)

  7. The grading score of the elastography of lymph nodes. [ Time Frame: 15 minutes ]
    grading score (The percentage of the number of specific color pixels in the total number of pixels of the entire lymph node image:1 point: over 80% of the section was non blue (green, yellow and red); 2 point: more than 50%, but less than 80% of the section was non-blue (green, yellow and red);3 point: more than 50%, but less than 80% of the section was blue; and 4 point: over 80% of the section was blue)


Other Outcome Measures:
  1. The short diameter of the enhanced chest computed tomography of lymph nodes. [ Time Frame: 30 minutes ]
    short diameter (millimeter,mm)

  2. The texture of the enhanced chest computed tomography of lymph nodes. [ Time Frame: 6 minutes ]
    texture (homogeneous or not)

  3. The shape of the enhanced chest computed tomography of lymph nodes. [ Time Frame: 6 minutes ]
    shape (round or not)

  4. The boundary of the enhanced chest computed tomography of lymph nodes. [ Time Frame: 6 minutes ]
    boundary (clear or not)

  5. The mean CT value of the enhanced chest computed tomography of lymph nodes. [ Time Frame: 6 minutes ]
    mean CT value(hounsfield unit,HU)



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Ages Eligible for Study:   27 Years to 81 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Patients who have enlarged intrathoracic lymph nodes(≥1cm) evaluated by chest enhanced CT and/or 18-FDG high uptake (SUV Max > 2.5) evaluated by 18-FDG PET-CT.
  2. Patients who are willing to undergo electronic bronchoscopy and agreed to take TBNA and EBUS-TBNA for pathology.

Exclusion Criteria:

  1. There is a contraindication of electronic bronchoscopy: activity of hemoptysis, hypertension and arrhythmia, recent myocardial infarction or unstable angina pectoris attacks, serious heart and lung dysfunction, bleeding tendency which cannot be corrected, serious obstruction of superior vena cava syndrome, suspected aortic aneurysm, multiple pulmonary bullous,the body condition is extremely exhaustion, the pregnant or lactation period women, the infected wound deferred, uncontrollable mental illness.
  2. Patients who are not willing to accept electronic bronchoscopy.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03391557


Sponsors and Collaborators
Fangsurong
Johns Hopkins University
Investigators
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Principal Investigator: Wei Gu, master The First Affiliated Hospital with Nanjing Medical University
Publications:

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Responsible Party: Fangsurong, Deputy chief physician, master, Nanjing First Hospital, Nanjing Medical University
ClinicalTrials.gov Identifier: NCT03391557    
Other Study ID Numbers: YL20160713-020
First Posted: January 5, 2018    Key Record Dates
Last Update Posted: January 25, 2018
Last Verified: January 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: We are willing to share data related to lymph nodes in patients who were involved in the study. Researchers can contact us via mail to get data information for further research if they would.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Clinical Study Report (CSR)
Time Frame: The data is available now and in 3 years.
Access Criteria: Researchers who are involved in the study of ultrasound elastography with lymph nodes and contact contact us via mail until our agreement.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Fangsurong, Nanjing First Hospital, Nanjing Medical University:
Elastography
Lymph node
Diagnosis