Lung Cancer, Adenocarcinoma Clinical Trial
Official title:
Low-dose Protocol for Computed Tomography-guided Lung Biopsy
Verified date | June 2019 |
Source | Xuzhou Central Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare the diagnostic accuracy and complication rate between low-dose computed tomography-guided and standard-dose computed tomography-guided lung biopsy.
Status | Completed |
Enrollment | 280 |
Est. completion date | May 31, 2019 |
Est. primary completion date | May 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Non-diagnostic lung lesions; Solid lung lesions; Lesion size = 5mm. Exclusion Criteria: - The lesion which has been punctured previously; Severe dysfunction in heart, lung and coagulation function. |
Country | Name | City | State |
---|---|---|---|
China | Xuzhou Central Hospital | Xuzhou | Jiangsu |
Lead Sponsor | Collaborator |
---|---|
Xuzhou Central Hospital |
China,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Diagnostic accuracy | Diagnostic accuracy is defined as the biopsy diagnosis matches with the final diagnosis. The final diagnosis is made according to the surgical or follow-up findings. | From the date of randomization until the date of first documented final diagnosis, assessed up to 24 months | |
Secondary | Complication | Biopsy-related complications mainly include pneumothorax and hemoptysis. Complications is evaluated by computed tomography scan and clinical symptoms. | From the date of randomization until the date of first documented biopsy-related complication, assessed up to 1 day. |