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Pulmonary Nodule, Solitary clinical trials

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NCT ID: NCT03181490 Completed - Clinical trials for Pulmonary Nodule, Solitary

Circulating Tumor DNA Methylation Test to Differentiate Benign and Malignant Pulmonary Nodules

Start date: June 8, 2017
Phase:
Study type: Observational

Current state-of-the-art lung cancer early screening utilizes low-dose CT scan to identify lung nodules smaller than 3 cm in diameter. However, it's still a clinical challenge to differentiate between malignant and benign nodules. In previous studies, the investigators had taken the approach of methylation profiling by high throughput bisulfite DNA sequencing in tissue samples to identify specific methylation signatures. The investigators had learned methylation patterns that differentiate malignant vs. benign lesions from tissue samples by in-depth data mining, and then used pattern matching to classify plasma samples. In this study, the investigators are going to validate the efficacy of ctDNA methylation test for diagnosing early lung cancer by comparing results of the pre-surgery ctDNA methylation test with the post-surgery pathology.

NCT ID: NCT03097627 Completed - Clinical trials for Pulmonary Nodule, Solitary

Intravenous Indocyanine Green for Localization of Intra-thoracic Lesions

Start date: February 1, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This is a clinical trial to evaluate the intravenous administration of indocyanine green (ICG) as a method of intra-thoracic lesion localization. The primary purpose is to determine if intravenous ICG allows us to identify intra-thoracic lesions.

NCT ID: NCT00963651 Completed - Clinical trials for Pulmonary Nodule, Solitary

GE Healthcare VolumeRAD Lung Nodule Detection Study

Start date: August 2009
Phase: N/A
Study type: Observational

To perform a multiple reader, multiple case (MRMC) observer study assessing the detection performance of VolumeRAD tomosynthesis of the chest in detecting lung nodules.

NCT ID: NCT00841750 Recruiting - Clinical trials for Lung Diseases, Interstitial

Chest Tube After a Video-assisted Thoracoscopic Surgery Pulmonary Wedge Resection

NOTUBE
Start date: July 2008
Phase: Phase 3
Study type: Interventional

After performing VATS pulmonary wedge resections, a chest tube is routinely left in the pleural cavity to drain possible air leaks and fluid accumulations. Chest tubes after VATS pulmonary wedge resections are left in place a minimum of 1 day. However, this practice has no scientific foundations. The investigators believe it is possible to avoid the placement of a chest tube after this procedure in a great amount of patients. This is a randomized controlled clinical trial with analysis blinding in which the investigators want to compare the outcomes between installing a chest tube or not after VATS pulmonary wedge resections. The investigators will include consecutively patients with interstitial lung disease or indeterminate pulmonary nodules undergoing this procedure, at the participating institutions. The investigators calculated a sample size of 50 subjects in each group using pneumothorax < 10% data from Luckraz et al and to determine a difference of hospital stay of 2 versus 1 day; DS(1.5), power = 0.9 and alpha = 0.05.