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Lung Neoplasms clinical trials

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NCT ID: NCT01795352 Completed - Clinical trials for EGFR Mutated Non-small Cell Lung Cancer Patients

Retrospective Study in a NSCLC M+ p

Ca_Pulmon
Start date: March 2013
Phase: N/A
Study type: Observational

This is a national, multicentre, non-interventional, retrospective study to be carried out in the oncology settings of approximately 15-20 Spanish hospitals. At each participant hospital, all patients recently diagnosed with advanced EGFR mutated NSCLC (both newly or with recurrent disease , without previous treatment for metastatic disease) from April 2010 to December 2011 will be included as study population. Information about the follow-up of the patients during a minimum of 12 months after diagnosis will be collected.

NCT ID: NCT01793246 Completed - Lung Neoplasms Clinical Trials

Registry Trial to Determine pCLE Image Interpretation Criteria and Preliminary Accuracy in the Lung

BREATH
Start date: February 2013
Phase: N/A
Study type: Observational

Patients will be enrolled that are undergoing bronchoscopy for diagnosis of discrete lung lesions or for detection of acute rejection following lung transplants. The hypothesis is that bronchoscopy together with probe-based endomicroscopy (pCLE)results in improved and/or incremental diagnostic yield (definitive diagnosis) over conventional bronchoscopy.

NCT ID: NCT01793155 Completed - Lung Cancer Clinical Trials

Effects of Inspiratory Muscle Training After Lung Cancer Surgery, a Randomized Controlled Trial

Start date: November 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of postoperative inspiratory muscle training on the recovery of respiratory muscle strength in high risk patients referred for lung cancer surgery. Furthermore, to assess longitudinal changes in respiratory muscle strength, physical capacity and health-related quality of life after lung cancer surgery

NCT ID: NCT01792479 Completed - Clinical trials for Non-small Cell Lung Cancer

A Phase 2 Study to Determine the Safety and Efficacy of BIND-014 (Docetaxel Nanoparticles for Injectable Suspension) as Second-line Therapy to Patients With Non-Small Cell Lung Cancer

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of BIND-014 in patients with advanced non-small cell lung cancer (NSCLC).

NCT ID: NCT01790217 Completed - Clinical trials for Non-Squamous Non-Small Cell Lung Cancer

An Observational Study of Tarceva (Erlotinib) in First Line in Patients With Advanced EGFR Mutation-Positive Non-Small Cell Lung Cancer (GERTAC)

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

This observational study will evaluate the efficacy and safety of Tarceva (erlotinib) in first-line therapy in patients with locally advanced or metastatic EGFR mutation-positive non-small cell lung cancer. Eligible patients, for whom the treating physician has decided to initiate treatment with Tarceva according to the local label will be followed for 18 months.

NCT ID: NCT01786187 Completed - Lung Cancer Clinical Trials

The Symptom Experience Study in Persons With Non-Small Cell Lung Cancer

SES
Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Little is known about the symptom experience of persons having undergone surgery for lung cancer. What we do know is that symptoms are common and can become severe and lasting. The main purpose of this study is two-fold: 1. To better understand the symptom experience of persons with lung cancer prior to surgery and for up to six weeks after returning home from the hospital. 2. To examine the role of a light physical activity program in persons who are undergoing surgery for lung cancer for the treatment of a specific symptom. The goals of this study include: - Collecting information about the participant's current and prior health history, symptoms, and health-related quality of life. - Assessing our ability to recruit participants to the study. - Assessing participant's level of participation. - Evaluating the participant's satisfaction with the program. We expect that patients after undergoing surgery for lung cancer during the recovery process will experience multiple symptoms. We also expect to find that a light intensity physical activity program will be feasible, acceptable, and show a positive impact on symptoms such as cancer-related fatigue and confidence for cancer-related fatigue self-management. Information gained from this randomized controlled trial study will be used to refine the design of future larger-scale studies targeting symptoms such as cancer-related fatigue for the lung cancer population.

NCT ID: NCT01785342 Completed - Lung Cancer Clinical Trials

DECAMP-1: Diagnosis and Surveillance of Indeterminate Pulmonary Nodules

DECAMP-1
Start date: January 2013
Phase:
Study type: Observational

The goal is to improve the efficiency of the diagnostic follow-up of patients with indeterminate pulmonary nodules by determining whether biomarkers for lung cancer diagnosis that are measured in minimally invasive biospecimens are able to distinguish malignant from benign pulmonary nodules that are incidentally detected in high-risk smokers.

NCT ID: NCT01784640 Completed - Clinical trials for Stage IV Non-small Cell Lung Cancer

Pemetrexed Disodium and Hsp90 Inhibitor AUY922 in Treating Patients With Previously Treated Stage IV Non-Small Cell Lung Cancer

Start date: January 31, 2014
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and the best dose of Hsp90 inhibitor AUY922 when given together with pemetrexed disodium in treating patients with previously treated stage IV non-small cell lung cancer. Hsp90 inhibitor AUY922 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as pemetrexed disodium, work in different ways to stop the growth of tumor cell, either by killing the cells or stopping them from dividing. Giving Hsp90 inhibitor AUY922 together with pemetrexed disodium may kill more tumor cells

NCT ID: NCT01781988 Completed - Lung Cancer Clinical Trials

Personalized Therapy in Non-small Cell Lung Cancer

PTINCLC
Start date: June 2009
Phase: Phase 2
Study type: Interventional

Excision repair cross complementing 1 (ERCC1) ribonucleotide reductase M1 (RRM1) and thymidylate synthase(TS) are molecular determinants that predict sensitivity or resistance to platinum agents 、 gemcitabine and pemetrexed respectively. Tailored therapy using these molecular determinants suggested patient benefit in a previously reported phase 2 trial. Here, we designed a study for an individual patient analysis of prospectively accrued patients who were treated with the "personalized therapy" approach versus other standard approaches.

NCT ID: NCT01781741 Completed - Clinical trials for Stage IV Non-small Cell Lung Cancer

Stereotactic Body Radiation Therapy After Surgery in Treating Patients With Stage III-IV Non-small Cell Lung Cancer

Start date: March 6, 2013
Phase: Early Phase 1
Study type: Interventional

This pilot clinical trial studies stereotactic body radiation therapy after surgery in treating patients with stage III-IV non-small cell lung cancer. Stereotactic radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue. Lymphadenectomy may remove tumor cells that have spread to nearby lymph nodes in patients with non-small cell lung cancer. Giving stereotactic body radiation therapy after lymphadenectomy may kill any tumor cells that remain after surgery.