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Bronchogenic Carcinoma clinical trials

View clinical trials related to Bronchogenic Carcinoma.

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NCT ID: NCT00652769 Completed - Clinical trials for Bronchogenic Carcinoma

A New Pathway With BronchOscopic or Oesophageal Ultrasound for Lung Cancer Diagnosis and STaging (BOOST)

BOOST
Start date: March 2008
Phase: Phase 3
Study type: Interventional

In the UK, staging of lung cancer is time consuming (taking on average more than 3 weeks), costly and inaccurate in up to 20% of cases. The investigators wish to determine whether using the newer techniques of endobronchial ultrasound (EBUS) and endoscopic ultrasound (EUS) improves lung cancer staging. The investigators' hypothesis is that EUS (endoscopic ultrasound) or EBUS (endobronchial ultrasound guided transbronchial needle aspirate) as a first test after CT scan in the diagnosis and staging of lung cancer will result in a reduction in the time from first outpatient appointment to treatment decision, a reduction in the total number of scans and investigative operations, fewer outpatient attendances and a reduction in healthcare costs.

NCT ID: NCT00407264 Completed - Clinical trials for Bronchogenic Carcinoma

Randomized Trial of Fluticasone in Bronchial Premalignancy

Start date: February 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy of fluticasone on the development of lung cancer in smokers

NCT ID: NCT00001515 Completed - Clinical trials for Chronic Granulomatous Disease

Diagnostic Effectiveness of Virtual Bronchoscopy

Start date: December 1995
Phase: Phase 1
Study type: Interventional

This study will evaluate a new technique for examining the air passages of the lungs called "virtual bronchoscopy." It involves using computed tomography (CT) images of the chest to generate a 3-dimensional model of the walls of the trachea and bronchi (airway passages). This non-invasive method lets doctors see small masses and areas of narrowing in the passages without having to do surgery or pass a tube through them. Patients with diseases of the air passages who are enrolled in an NIH clinical trial may participate in this study, which requires having a CT scan. The patient lies on a table that slowly slides into a hole in a donut-shaped X-ray machine (the scanner). Patients may have to hold their breath several times during the procedure. Some patients may be given an injection of a contrast agent through a catheter (thin tube) placed in an arm vein to improve visibility of abnormalities. Patients may also be asked to breathe oxygen through nasal prongs to allow them to hold their breath longer. The procedure usually takes 15 to 20 minutes.