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Multiple Pulmonary Nodules clinical trials

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NCT ID: NCT03338049 Completed - Lung Cancer Clinical Trials

All in One Study: A Prospective Trial of Electromagnetic Navigation for Biopsy of Pulmonary Nodules

AIO
Start date: February 14, 2018
Phase: N/A
Study type: Interventional

This is a multi-center, non-randomized, single-arm, prospective trial to evaluate a staged sampling methodology designed to maximize the diagnostic yield of lung biopsy in a single procedure setting.

NCT ID: NCT03320044 Completed - Carcinoma Clinical Trials

Early Diagnosis of Small Pulmonary Nodules by Multi-omics Sequencing

Start date: October 18, 2017
Phase:
Study type: Observational

Analyse immune repertoire and genetic mutations of benign and malignant pulmonary nodule,and evaluate peripheral blood detection for identifying nature of pulmonary nodule.

NCT ID: NCT03305978 Completed - Lung Cancer Clinical Trials

Pulmonary Nodule Detection: Comparison of an Ultra Low Dose vs Standard Scan.

npUBD
Start date: September 26, 2017
Phase: N/A
Study type: Interventional

Lung cancer screening programs are still discussed in Europe today, and one of the concern is radiation due to iterative CT. The aim of this monocentric, prospective, non randomized study is to compare an ultra low dose chest CT (approaching a two views X ray) versus a standard low dose chest CT for ≥4mm lung nodules detection, and secondary for lung nodule characterization and smoking associated findings (emphysema, bronchial abnormalities and coronary calcifications).

NCT ID: NCT03293433 Completed - Pulmonary Cancer Clinical Trials

Quantification of microRNAs in Diagnosis of Pulmonary Nodules

miR-Nod
Start date: November 2015
Phase:
Study type: Observational

One of the main challenges of thoracic oncology lies in earlier diagnosis of lung cancer to improve survival rate, wich is about 15% at 5 years. This poor prognosis is often linked to late diagnosis. Efforts are being made worldwide to offer testing in patients at risk or earlier diagnosis of lung cancer in order to offer the patient curative treatments. Indeed, supported at the stage of nodule (less than 3 cm lesion), lung cancer is curable by surgery in 80% of patients. Nevertheless, there are many differential diagnoses and access to these lesions is often difficult and risky. In this context, the management of pulmonary nodules, which can be either benign lesions or beginners cancers, is a real challenge for pulmonologists and thoracic oncologists every day: it is important not to disregard a potentially operable nodule and avoiding offer patients invasive procedures for benign nodules. Indeed, many procedures (endoscopy, puncture under scanner, thoracotomy) are made to determine if suspicious nodules are benign or not. In the large National Lung Screening Trial, 28% of the procedures were associated with complications (including 11% classified severe and 16 deaths). It is therefore essential to develop non-invasive tools to refine treatment decisions.

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: NCT03159377 Completed - Clinical trials for Pulmonary Nodule, Multiple

Ultra-Low Dose CT Denoising for Lung Nodule Detection

Start date: July 4, 2017
Phase:
Study type: Observational

We will perform an ultra low-dose CT (ULDCT) in addition to a regular chest CT scan for adult patients undergoing a clinically indicated chest CT. Using a recently developed computationally efficient algorithm for the denoising of ULDCT scans after image reconstruction, we will compare the sensitivity, specificity and accuracy of lesion detection with the ULDCT as compared to the regular CT scan.

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: NCT03086213 Completed - Clinical trials for Peripheral Solitary Pulmonary Nodule or Tuberculoma

Comparative Study of Nonintubated Uniport Thoracoscopic Surgery Using Thoracic Paravertebral Nerve Block Versus Intercostal Nerve Block for Peripheral Solitary Pulmonary Nodule Patients

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to study the safety and effectiveness of the effects on the perioperative pain control comparing between the thoracic paravertebral nerve block using the camera guided and the intrathoracic intercostals nerve block for the management of nonintubated local regional analgesia in uniport thoracoscopic surgery for the undetermined solitary nodules patients.

NCT ID: NCT02952261 Completed - Lung Neoplasm Clinical Trials

Application of 3D Printing Technique in Small Pulmonary Nodule Localization

Start date: October 24, 2016
Phase: N/A
Study type: Interventional

The trial is to evaluate the efficacy and safety of three-dimensional printed navigational template in the clinical application of small peripheral lung nodule localization.

NCT ID: NCT02851368 Completed - Clinical trials for Solitary Pulmonary Nodules

Near Infrared Fluorescence Imaging With Indocyanine Green

NIFI-ICG
Start date: November 2016
Phase: Early Phase 1
Study type: Interventional

This research study will evaluate how Near Infrared Fluorescence imaging (NIFI) with indocyanine green (ICG) contrast dye can assist in the identification and diagnosis of lung nodules during surgery. NIFI is an intraoperative imaging technology that utilizes a coupled camera/fluorophore (ICG) system to fluoresce tissues of interest. Intravenous ICG is a fluorophore with a long-standing high safety profile.