Clinical Trials Logo

Lung Cancer clinical trials

View clinical trials related to Lung Cancer.

Filter by:
  • Enrolling by invitation  
  • « Prev · Page 3

NCT ID: NCT01551082 Enrolling by invitation - Lung Cancer Clinical Trials

Outpatient Chest Tube Management Following Thoracic Resection Improves Patient Length of Stay and Satisfaction Without Compromising Outcomes

Start date: March 2012
Phase: N/A
Study type: Observational

Discharging patients home with air leak and chest tube to portable drainage device after thoracic resection is cost effective and safe without compromising patients outcome or satisfaction. Despite good outcomes this practice is not done universally by thoracic surgeons.

NCT ID: NCT01460264 Enrolling by invitation - Lung Cancer Clinical Trials

An Open Prospective Longitudinal Pulmonary-cardiovascular Cohort Study

BIG3
Start date: October 16, 2013
Phase:
Study type: Observational

This is an observational study aiming to identify and validate biomarkers (including imaging and clinical descriptors) for chronic obstructive pulmonary disease (COPD), cardiovascular disease (CVD) and lung cancer.

NCT ID: NCT01385722 Enrolling by invitation - Lung Cancer Clinical Trials

Molecular Analysis of Thoracic Malignancies

Start date: August 2011
Phase:
Study type: Observational

A research study to learn about the biologic features of cancer development, growth, and spread. We are studying components of blood, tumor tissue, normal tissue, and other fluids, such as urine, cerebrospinal fluid, abdominal or chest fluid in patients with cancer. Our analyses of blood, tissue, and/or fluids may lead to improved diagnosis and treatment of cancer by the identification of markers that predict clinical outcome, markers that predict response to specific therapies, and the identification of targets for new therapies.

NCT ID: NCT00966511 Enrolling by invitation - Lung Cancer Clinical Trials

Vibration Response Imaging (VRI) in Patients Who Are Potential Candidates for Surgical Resection

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

The primary purpose of the study is to investigate the use of VRI to guide the selection of patients for lung surgery. Perfusion scintigraphy is the current method to assess the fractional contribution of lung function of the remaining lung. The hypothesis is that VRI can determine quantitative postoperative lung function equally accurately as a quantitative perfusion scan.

NCT ID: NCT00026754 Enrolling by invitation - Breast Cancer Clinical Trials

Eligibility Screening for the NIH Intramural Research Program Clinical Protocols

Start date: January 14, 2004
Phase:
Study type: Observational

The purpose of this protocol is to provide patients with adequate informed consent to understand that screening tests with minimal health risk will be performed to evaluate their eligibility for a research study. The protocol makes it clear that patients initial visit to the intramural clinical program may include screening studies that are not medically necessary for disease management, but are done purely for research purposes. Patients with a known or suspected diagnosis of cancer, HIV infection, skin disorder or immunodeficiency who are being considered for enrollment in a National Cancer Institute intramural clinical research protocol will participate in this consent protocol. It informs patients of screening tests and procedures involving minimal risk that are done for research purposes only, including blood tests, electrocardiogram, standard X-rays (e.g., chest X-ray), bone films, computed tomography (CT), magnetic resonance imaging (MRI), and nuclear medicine studies. It explains that other eligibility screens that are more invasive and involve greater risk, such as a biopsy, will require separate consent.