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Lung Cancer clinical trials

View clinical trials related to Lung Cancer.

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NCT ID: NCT02363101 Not yet recruiting - Lung Cancer Clinical Trials

Health Outcomes and Costs (HOC) in Lung Cancer (LC)

HOC-LC
Start date: March 2015
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the costs, health-related quality of life and preference values from lung cancer patients assisted in a Brazilian public health care unit.

NCT ID: NCT02362776 Completed - Breast Cancer Clinical Trials

Metabolic Changes as a Diagnostic Indicator for Cancer

Start date: October 2009
Phase: N/A
Study type: Observational [Patient Registry]

This study aims to determine whether metabolic changes occur in blood plasma of cancer patients, and whether these changes can be used as a biomarker to detect cancer. These analyses will be done by means of nuclear magnetic resonance (NMR) spectroscopy.

NCT ID: NCT02362204 Recruiting - Lung Cancer Clinical Trials

Lung Cancer Nurse Model: a Phase II Study

LCN-II
Start date: January 2015
Phase: N/A
Study type: Observational

Lung cancer patients experience significant physical symptoms, psychological distress and have many supportive care needs that impact on quality of life. Implementing the role of a Lung Cancer Nurse (LCN) is a response to meet the needs of patients and caregivers. Primary aim is to assess the feasibility of a LCN intervention and feasibility to collect longitudinal patient self-assessment questionnaires at the Thoracic Cancer Centre of the University Hospital of Lausanne. Secondary aims are: i) to describe self-reported changes in self-efficacy, symptoms and unmet supportive care needs across three time points during the first line therapy and ii) to explore professional acceptability of the new LCN model evaluating the perceptions of barriers and facilitators of the model by the LCN and the other multidisciplinary members of the comprehensive lung cancer care team. An exact single-stage (no interim analysis) design will be applied to determine feasibility for further studies to be undertaken. Secondary outcomes will be analyzed descriptively at each data collection (Baseline, Time1, Time2) time point and professional acceptability will be explored by focus groups with selected members of the interdisciplinary team.

NCT ID: NCT02361099 Completed - Lung Cancer Clinical Trials

SENTINEL : Impact of the Use of a Web-application for the Detection of Lung Cancer Relapse

SENTINEL
Start date: June 3, 2014
Phase: Phase 3
Study type: Interventional

This is a study that evaluates an optimization of the monitoring of patients with lung cancer in order to extend the survival of patients by improving their quality of life and decreasing anxiety generated by the achievement of balance sheets imaging. The spacing of the follow-up imaging also helps to reduce the cost of such monitoring. The main objective of this study is to evaluate the overall survival of patients.

NCT ID: NCT02357992 Completed - Lung Cancer Clinical Trials

Lung Cancer STARS Trial - STARS Revised Clinical Trial Protocol: Stereotactic Ablative Radiotherapy (SABR) in Stage I Non-small Cell Lung Cancer Patients Who Can Undergo Lobectomy

Start date: April 5, 2010
Phase: N/A
Study type: Interventional

The goal of this clinical research study is to evaluate the outcome of a standard radiation treatment called stereotactic radiotherapy (SRT) for NSCLC. Specifically, researchers want to learn if standard SRT has as good of an outcome at 3 years after the procedure. The safety of the study treatment will also be analyzed.

NCT ID: NCT02350361 Recruiting - Lung Cancer Clinical Trials

Endostar Combination With Chemotherapy and EGFR-TKI in Lung Cancer Rechallenging Treatment After Acquired Resistance.

Start date: January 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Here we are going to find a method by using available multiple drugs including angiogenesis medicine - Endostar to treat lung cancer patients who acquired resistence from EGFR-TKI but have responsed to it before.

NCT ID: NCT02349724 Recruiting - Breast Cancer Clinical Trials

A Clinical Research of CAR T Cells Targeting CEA Positive Cancer

Start date: December 2014
Phase: Phase 1
Study type: Interventional

The main purpose of this research is to verify the safety of CEA targeted chimeric antigen receptor T cells and to determine the proper dosage of CAR T cells infused.

NCT ID: NCT02347839 Recruiting - Lung Cancer Clinical Trials

NEoadjuvant Gefitinib fOllowed by Surgery and gefiTinib In unresectAble sTage III NSCLC With EGFR Mutations.

NEGOTIATE
Start date: January 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to studying neoadjuvant gefitinib followed by surgery, followed by adjuvant gefitinib to see how well it works in treating patients with unresectable stage III NSCLC harboring EGFR mutations.

NCT ID: NCT02346318 Recruiting - Lung Cancer Clinical Trials

The Randomized Controlled Clinical Trial of Kushen Injection

Start date: November 2014
Phase: Phase 4
Study type: Interventional

The randomized controlled multicenter clinical study of compound Kushen Injection to reduce the radiotherapy related adverse reactions in lung cancer is a phase Ⅳ clinical trials,The main purpose is to evaluate the effect of compound Kushen Injection in preventing and reducing the radiotherapy related adverse reactions. The participants of the clinical trials are patients with lung cancer who need thoracic radiotherapy. In clinical trials, one group of participants is given compound Kushen Injection with chemoradiotherapy, while another group is only given chemoradiotherapy. The period of trials is 18 months.

NCT ID: NCT02341170 Withdrawn - Lung Cancer Clinical Trials

HS-PCI in Locally Advanced Adenocarcinoma of the Lung

HIPPO-S
Start date: January 2016
Phase: N/A
Study type: Interventional

The primary aim of this study is evaluate the impact of hippocampal-sparing prophylactic cranial irradiation (HS-PCI) on survival status in patients with nodal-positive (locally advanced) adenocarcinoma by comparing overall survival rates of patients undergoing HS-PCI to that of patients without this intervention. In addition, this study aims to investigate whether HS-PCI is detrimental on neurocognitive function and to evaluate its impact on the patient's quality of life.