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Lung Cancer clinical trials

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NCT ID: NCT01172041 Completed - Lung Cancer Clinical Trials

The Role of Audiovisual Biofeedback on Image Quality During 4D Anatomic and Functional Imaging

Start date: July 2010
Phase: N/A
Study type: Observational

This study will investigate whether audiovisual biofeedback, in which visual and audio cues are used to regulate the patient's breathing, can increase the image quality of 4D CT and 4D PET scans.

NCT ID: NCT01172028 Completed - Breast Cancer Clinical Trials

Pemetrexed Disodium and Docetaxel in Treating Patients With Advanced Solid Tumors

Start date: September 2005
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells of by stopping them from dividing. Pemetrexed disodium may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase I trial is studying the side effects and best dose of giving pemetrexed disodium and docetaxel together in treating patients with advanced solid tumors.

NCT ID: NCT01165658 Terminated - Lung Cancer Clinical Trials

Study of Hypofractionated Proton Radiation Therapy in Thoracic Malignancies

Start date: July 16, 2010
Phase: Phase 1
Study type: Interventional

The goal of this clinical research study is to study the safety of giving larger daily doses of proton radiation therapy than the standard dose levels given to treat lung cancer. Researchers want to find the highest daily dose of proton radiation that can be given without having to stop therapy due to side effects.

NCT ID: NCT01160731 Withdrawn - Lung Cancer Clinical Trials

Panobinostat, Etoposide, and Cisplatin as First-Line Therapy in Treating Patients With Extensive-Stage Small Cell Lung Cancer

Start date: November 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Panobinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as etoposide and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving panobinostat together with etoposide and cisplatin may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of panobinostat when given together with etoposide and cisplatin as first-line therapy in treating patients with extensive-stage small cell lung cancer.

NCT ID: NCT01158495 Completed - Lung Cancer Clinical Trials

Outcome Measures in Infant/Early Childhood Lung Disease w/ Chest CT Scanning & Lung Function Testing

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

To implement a new method of performing chest CT imaging in young children at Packard Children's Hospital entitled controlled ventilation infant/young child chest CT scanning. This technique will be used to evaluate early lung disease comparing quantitative chest CT air trapping and airway measurements with lung function measurements in infants, toddlers, and young children with chronic lung disease.

NCT ID: NCT01158456 Completed - Lung Cancer Clinical Trials

Metabolism of NNK Among African Americans

Project 5
Start date: December 2010
Phase:
Study type: Observational

Metabolism and DNA adduct formation are critical in cancer induction by NNK. The investigators goal is to understand whether the observed ethnic/racial differences in lung cancer incidence are due to variations in NNK metabolism. The investigators overall hypothesis is that cancer susceptibility relates to carcinogen dose and to the balance between carcinogen metabolic activation and detoxification. The investigators propose to test this hypothesis via investigation of potential differences in NNK metabolic activation and detoxification in African American and European American smokers.

NCT ID: NCT01152463 Completed - Lung Cancer Clinical Trials

Sonography After Thoracic Surgery (SATS)

Start date: June 2010
Phase: N/A
Study type: Observational

Lung cancer remains the leading cause of mortality from malignant diseases in both men and women worldwide. Following thoracic surgery and pulmonary resection, patients have a surgically induced pneumothorax / hydro-hemothorax and hence tube thoracostomy is necessary to drain the air and effusion. Due to this, patients must undergo post-operative chest x-ray (CXR) evaluations in order to evaluate the chest and make decisions regarding removal of chest tubes (CT) as well as for decisions regarding patient discharge. Thoracic Ultrasound (US) has been shown to be accurate at diagnosing pneumothorax and has been well-studied in the trauma population. To the investigators knowledge, there are currently no centers using thoracic US routinely in the post-operative setting following thoracic surgery.

NCT ID: NCT01147965 Completed - Breast Cancer Clinical Trials

Active Immunotherapy CEA Vaccine in Patients With Malignancies Expressing CEA

Start date: June 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find out what effects (good and bad) that a cancer vaccine has on you and your cancer. The cancer vaccine is called Ad5 [E1-, E2b-]-CEA(6D)or ETBX-011 and is made by Etubics. This vaccine is based on a virus called an adenovirus but it has been changed to express the protein CEA that is found on some cancer cells. Therefore, the vaccine can tell the immune system to attack cancer cells which make CEA. The investigators are trying to determine whether giving this virus is safe and whether this causes a strong immune system attack on the cancer. ETBX-011 is an investigational drug.

NCT ID: NCT01147562 Active, not recruiting - Lung Cancer Clinical Trials

Biomarker Discovery and Validation in Lung Cancer

LCS
Start date: October 14, 2009
Phase: N/A
Study type: Interventional

Lung cancer is responsible for the most deaths due to cancer each year in both men and women worldwide and once diagnosed, the 10 year survival rate is poor (<15%). This poor prognosis is based in large part on the absence of an effective diagnostic test for the disease. The chief objective of this study is to develop a molecular-based diagnostic test specific for lung cancer. Subjects suspected or diagnosed with lung cancers, who are either undergoing thoracentesis, biopsy of a suspicious lesion or surgical resection of their tumor will be asked to participate in this study. Those subjects, who will undergo surgical resection, will donate both lung tumor tissue and adjacent normal lung tissue (potentially including lymph nodes), while non-surgical candidates will donate a portion of their excess biopsy sample, if available, after diagnosis has been confirmed. Subjects undergoing thoracentesis for pleural effusion will donate a portion of their fluid sample, if the fluid volume collected is in excess of that needed for clinical care purposes. Blood samples and optionally saliva will also be collected from all subjects, whether undergoing surgery or not. In addition to biosample collection, detailed annotated demographic and clinical information will be collected from subjects. Subjects will be followed for outcome analysis, specifically for tumor recurrence, every 6 months, during 5 years. In case of change in chemotherapy treatment, biosamples and clinical information will also be collected. Collected biosamples will be analyzed using a series of molecular and proteomic technologies for developing biomarkers of the disease.

NCT ID: NCT01145924 Unknown status - Lung Cancer Clinical Trials

Transbronchial Needle Forceps for Endobronchial Ultrasound

Start date: January 2010
Phase: Phase 2
Study type: Interventional

Prove the feasibility of a needle forceps in patients with enlarged mediastinal lymph nodes