- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03288662
Relationship Between Computed Tomography Manifestation and Histopathological Classification of Thymic Epithelial Tumors
Evaluate the Relationship Between Computed Tomography Manifestation and Histopathological Classification of Thymic Epithelial Tumors
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
- Introduction: the World Health Organization (WHO) has proposed a classification of histopathological thymic tumor and it significance in prognosis. Chest computed tomography (CT) is the most common method to evaluate thymic epithelial tumors before operation. Therefore, the question is to predict the histopathological type of thymic epithelial tumors before surgery based on CT-scan images , to help determine treatment strategy and prognosis. In Vietnam, there are no published literature on this issue.
Materials and methods:
2.1. Cross-sectional descriptive study on 53 patients with diagnosed of thymoma by CT and had postoperative histopathology results as thymic epithelial tumors
2.2. Time and Place: in Departement of CTVS, Military Hospital 103, Vietnam from 10/2013 to 7/2017.
2.3. methods:
study in chest CT scan:
- Measure the maximun diameter of the tumor
- The contour: smooth contour or irregular contour
- The shape: round, oval and plaque base on the ratio between long axis and short axis of the tumor
- Some other characteristics: Degree of enhancement, Level of drug absorbed, Calcification, Invasion the local organs and Capsular destruction.
Histopathological study: based on the 2004 WHO classification:
- Thymoma: type A, AB, B1, B2, B3
- Thymic carcinoma
- Data processing: use software Epi Info 2000.
Expectation of results
- Relationship between the size and histopathological type of thymic epithelial tumors.
- Comparison of some characteristics of the tumor on preoperative chest CT scans and histopathological type of thymic epithelial tumors
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- All of patient have a chest CT scan pre-operation and a result of thymic epithelial tumors postoperative histopathology
Exclusion Criteria:
- Incomplete or loss the CT and postoperative histopathology
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: CT and histopathological classification
With each histopathological type of thymic epithelial tumors, we measure the maximun diameter in chest CT scan.
Comparison of some characteristics of the tumor on preoperative chest CT scans and histopathological type of thymic epithelial tumors .
|
Cross-sectional descriptive study on 53 patients with diagnosed of thymoma by CT and had postoperative histopathology results as thymic epithelial tumors.
Base on the characteristics in Chest CT scan in each postoperative histopathology results.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
maximun diameter of the tumor
Time Frame: 1 month
|
Measure the maximun diameter of the tumor in chest CT scan
|
1 month
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Truong Giang Nguyen, PhD, VMMU
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LAnh
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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