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Multiple Pulmonary Nodules clinical trials

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NCT ID: NCT02653859 Not yet recruiting - Clinical trials for Solitary Pulmonary Nodule

Evaluate the Auxiliary Diagnostic Value of Circulating Tumor Cells in Benign and Malignant Lung Nodules

Start date: January 2016
Phase: N/A
Study type: Observational

By testing the CTC number of new solitary pulmonary nodule patient, evaluating the correlation of CTC number and benign and malignant lung nodules auxiliary diagnosis, the correlation of CTC number and the size of lung nodules of the malignant patients, the correlation between the CTC number and subtypes of malignant lung nodules patients.The CTC and tumor markers will be detected before the patient received treatment. Tumor markers include Pro-GRP, NSE, CEA, CYFRA211, SCC.

NCT ID: NCT02629978 Active, not recruiting - Neoplasms Clinical Trials

Radiofrequency Ablation of Malignant Pulmonary Nodules

Start date: October 2015
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the outcomes of radiofrequency ablation in the treatment of patients with malignant pulmonary nodules(not exceed 3cm )who are not suitable candidates for or refuse surgical resection.

NCT ID: NCT02623712 Active, not recruiting - Clinical trials for Carcinoma, Non-small-cell Lung

The Watch the Spot Trial

WTS
Start date: March 6, 2017
Phase: N/A
Study type: Interventional

This study will compare two clinically accepted protocols for surveillance imaging in individuals who are found to have a small pulmonary nodule on chest computed tomography (CT) scans.

NCT ID: NCT02602119 Completed - Neoplasms Clinical Trials

Intraoperative Imaging of Pulmonary Nodules by OTL38

Start date: May 2015
Phase: Phase 1
Study type: Interventional

The primary end-point of the study is to determine the sensitivity of OTL in identifying lung nodules when excited by an imaging probe. Investigators intend to enroll 300 lung cancer patients in this study. The study is focusing on patients presenting with suspected malignancies of the lung and pleura who are considered to be good surgical candidates.

NCT ID: NCT02531646 Enrolling by invitation - Clinical trials for Solitary Pulmonary Nodules

Clinical Evaluation of CARESTREAM Dual Energy and Digital Tomosynthesis

Start date: November 2015
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the imaging performance of Dual Energy and Digital Tomosynthesis (DE-DT) application against the commercially available predicate devices.

NCT ID: NCT02496624 Recruiting - Lung Cancer Clinical Trials

Cone-beam CT Guided Microcoil Localization of Pulmonary Nodules During Video Assisted Thoracic Surgery(VATS)

Start date: June 2015
Phase: N/A
Study type: Interventional

The Guided Therapeutics (GTx) program at the University Health Network is a network of clinicians, scientists, and engineers focused on the development and translation of image-guided technologies focused on minimally-invasive, adaptive therapies. Technologies developed within the GTx program include a portable intra-operative cone-beam CT (in collaboration with Siemens) that has been evaluated in clinical trials for head and neck surgery. The intraoperative imaging has been integrated with tracking and navigational tools and optical imaging to provide a general "surgical dashboard" that is used to improve the accuracy of surgical resection. A recent addition to the GTx program is the development of the GTx OR, located within the general operating room of the Toronto General Hospital. The GTx OR houses 2 complimentary advance technologies: the Siemens Zeego and the Siemens Somotom Flash CT. The dual-energy Somatom Flash provides a "gold-standard" in CT imaging, while the Zeego provides excellent 3D Cone-beam CT with robotic placement for flexible integration within the operating environment. Together, the integration of these 2 components into a single OR enables critical evaluation of the limits of CT imaging technology for surgical guidance. This study will be conducted using solely the Cone-beam CT (Zeego) for percutaneous placement and localization of markers for resection of small pulmonary nodules during VATS.

NCT ID: NCT02490059 Completed - Lung Cancer Clinical Trials

Ultrathin Bronchoscopy for Solitary Pulmonary Nodules

Babyscope
Start date: November 2000
Phase: Phase 4
Study type: Interventional

The evaluation of solitary pulmonary nodules (SPN) requires a balance between procedure-related morbidity and diagnostic yield, particularly in areas where tuberculosis is endemic. Data on ultrathin bronchoscopy (UB) for this purpose is limited. In this prospective randomised trial we compared diagnostic yield and adverse events of UB with standard-size bronchoscopy (SB) in a cohort of patients with SPN located beyond the visible range of SB.

NCT ID: NCT02468609 Recruiting - Pulmonary Emphysema Clinical Trials

Diagnostic Value of Ultralow-dose Computed Tomography for the Detection of Pulmonary Nodules and Lung Parenchym Alterations Compared to Standard-dose CT

RADFL
Start date: January 2015
Phase: N/A
Study type: Interventional

To investigate the diagnostic value of ultralow-dose computed tomography in the detection of pulmonary nodules and lung parenchym alterations (e.g. emphysema) compared to standard-dose-CT.

NCT ID: NCT02448225 Completed - Lung Carcinoma Clinical Trials

18F-FSPG PET/CT in Imaging Patients With Newly Diagnosed Lung Cancer or Indeterminate Pulmonary Nodules

Start date: June 16, 2015
Phase: Phase 2
Study type: Interventional

This clinical trial compares fluorine F 18 L-glutamate derivative BAY94-9392 (18F-FSPG) positron emission tomography (PET)/computed tomography (CT) to the standard of care fluorodeoxyglucose F-18 (18F-FDG) PET/CT in imaging patients with newly diagnosed lung cancer or indeterminate pulmonary nodules. PET/CT uses a radioactive glutamate (one of the common building blocks of protein) called 18F-FSPG which may be able to recognize differences between tumor and healthy tissue. Since tumor cells are growing, they need to make protein, and other building blocks, for cell growth that are made from glutamate and other molecules. PET/CT using a radioactive glutamate may be a more effective method of diagnosing lung cancer than the standard PET/CT using a radioactive glucose (sugar), such as 18F-FDG.

NCT ID: NCT02268162 Recruiting - Lung Neoplasms Clinical Trials

Diagnosis of Individuals With Pulmonary Nodules by Different Bronchoscopy Combination

Start date: April 2015
Phase: N/A
Study type: Interventional

This study evaluates the value of different bronchoscopy combination for diagnosing peripheral pulmonary lesions suspected to be cancer. One-third of participants will receive routine bronchoscopy, while one-third of participants will receive bronchoscopy combined with a guiding equipment and the other one-third of participants will receive bronchoscopy combined with two or more guiding equipments. These guiding equipments include virtual bronchoscopic navigation(VBN), endobronchial ultrasonography with a guide sheath(EBUS-GS) and fluoroscopy.