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Lung Neoplasms clinical trials

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NCT ID: NCT01885754 Recruiting - Clinical trials for Non-Small-cell Lung Cancer

Characterization of Peripheral Muscle Function in Patients With Non-small-cell Lung Cancer

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

Rationale: With 1.6 million new cases diagnosed each year and 1.3 million deaths, lung cancer is the leading cancer-related death worldwide and it represents a pressing health issue. Patients with lung cancer are more likely to experience cachexia, a severe debilitating disorder causing fatigue, weight loss, muscle wasting and associated with reduced physical function, increased chemotherapy toxicity and reduced survival. This syndrome occurring in about 80% of advanced cancer patients is the direct cause of death in about 20% of cases. However, despite the importance of cachexia in lung cancer, its mechanisms ans its relation with muscle function and effort tolerance are still unknown. Aim: To explore muscle function, signaling pathways and its relationship to impaired functional capacity of patients with non-small-cell lung cancer(NSCLC); depending of whether they have cachexic state at diagnosis. Methods: This study will be conducted at the Institut universitaire de cardiologie et de pneumologie de Québec. 56 patients newly diagnosed of NSCLC will be recruited and separated whether or not they have a cachexic state. The evaluation will need two visits separated by 5 days. During the evaluation the following tests will be done: - Anthropometric measures - Level of daily physical activity - Pulmonary function test - Maximal incremental cardiopulmonary exercise test on ergocycle - Endurance test on ergocycle - Muscle function tests - Magnetic stimulation - Quadriceps biopsy

NCT ID: NCT01884285 Completed - Clinical trials for Triple Negative Breast Cancer TNBC

AZD8186 First Time In Patient Ascending Dose Study

Start date: July 9, 2013
Phase: Phase 1
Study type: Interventional

This is a phase I, open-label, multicentre study of AZD8186 administered orally in patients with advanced castrate-resistant prostate cancer (CRPC), squamous non-small cell lung cancer (sqNSCLC), triple negative breast cancer (TNBC) and known PTEN-deficient/mutated or PIK3CB mutated/amplified advanced solid malignancies as monotherapy and in combination with abiraterone acetate or AZD2014.

NCT ID: NCT01883986 Completed - Lung Cancer Clinical Trials

Supportive Care for Patients Newly Diagnosed With Lung Cancer

Start date: February 2014
Phase: N/A
Study type: Interventional

The aims of this project are to assess the feasibility of recruiting patients and delivering a nurse-led telephone based palliative care intervention for patients with newly diagnosed lung cancer and to assess if among patients with newly diagnosed lung cancer, the investigators can estimate the effect of a nurse-led telephone based palliative care intervention on quality-of-life, symptom burden and patient satisfaction.

NCT ID: NCT01881906 Completed - Clinical trials for Small Cell Lung Cancer

Exercise in Advanced Stage Lung Cancer Patients

EXHALE
Start date: February 2012
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of twelve weeks of a physical and psycho-social program consisting of: supervised, structured exercise training in a group of advanced lung cancer patients (cardio and strength training, relaxation training) twice weekly. Primary outcome is (VO2peak). The hypotheses are that patients who undergo this intervention will increase maximal oxygen uptake (VO2peak), strength (1RM), functional capacity (6MWD) and quality of life (HRQOL) and reduce the level of anxiety and depression compared to those who do not.

NCT ID: NCT01881516 Not yet recruiting - Lung Cancer Clinical Trials

Acupuncture Research on Lung Cancer Patients With Cancer Related Fatigue(CRF)

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

we plan to conduct this trial to find out: - If acpuncture treatment could relieve CRF among lung cancer patients receiving chemo- or radio-therapy? - How about the extent it relieves?the safety and applicability ? - What's the possible influential factor and mechanism ?

NCT ID: NCT01880528 Completed - Clinical trials for Non-small Cell Lung Cancer

Lisinopril in Reducing Shortness of Breath Caused by Radiation Therapy in Patients With Lung Cancer

Start date: May 31, 2013
Phase: Phase 2
Study type: Interventional

This pilot clinical trial studies lisinopril in reducing shortness of breath caused by radiation therapy in patients with lung cancer. Lisinopril may decrease the side effects caused by radiation therapy in patients with lung cancer.

NCT ID: NCT01874678 Completed - Clinical trials for Non-small-cell Lung Cancer (NSCLC)

A Study of TS-1 Plus Cisplatin in Patients With Advanced Non-small-cell Lung Cancer

Start date: March 2011
Phase: N/A
Study type: Interventional

Objectives: 1. Primary Objective: To bridge the data of efficacy in term of overall response rate of TS-1 plus cisplatin in Taiwanese advanced NSCLC patients from that gained from Japanese population 2. Secondary Objectives: A. To assess progression free survival B. To assess overall survival C. To bridge the safety profile by assessing the toxicities and tolerability

NCT ID: NCT01872416 Recruiting - Clinical trials for Small Cell Lung Cancer

A Clinical Study of Liposomal Doxorubicin Combined With Ifosfamide Second-line Treatment in Small Cell Lung Cancer

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

At present, there is no standard second-line treatment of refractory and relapsed SCLC, topotecan, gemcitabine, paclitaxel, irinotecan and drugs such as cyclophosphamide second-line treatment of small cell lung cancer currently being explored, Anthracycline antibiotics is a cell cycle non-specific anticancer drugs could inhibit the synthesis of DNA, DNA and dependent RNA, its wide antitumor spectrum, widely used in malignant hematologic diseases and lung cancer and other solid tumors. Jacot W, et al evaluated epirubicin combined with ifosfamide (EI) for treatment of refractory and recurrent SCLC in 70 cases, the objective response rate (ORR) reached 21.4%, including 1 cases of complete remission, 10% other patients obtained stable disease (SD), all the patients had a median survival of 3.9 months, most (71%) patients with neutropenia, platelet count and anemia are also common, showed that EI treatment of refractory and relapsed SCLC is effectively controlled, toxicity. In view of epirubicin combined with ifosfamide (EI) scheme is effective and safety in the treatment of refractory and relapsed SCLC, the investigators will use liposomal doxorubicin plus ifosfamide second-line treatment of refractory and relapsed small cell lung cancer, may obtain better tumor remission rate, improve the prognosis of the patients.

NCT ID: NCT01872403 Recruiting - Clinical trials for Non-small Cell Lung Cancer

Neoadjuvant Chemotherapy of Nanoparticle Albumin-bound Paclitaxel/Carboplatin vs. Paclitaxel /Carboplatin in Stage Ⅱ B and IIIA Squamous Cell Carcinoma of the Lung

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

Albumin-bound paclitaxel plus carboplatin regimen in advanced NSCLC especially in lung squamous cell carcinoma has a better tumor response rate and safety, therefore.The main purpose of this study is to observe the safety and efficacy of albumin-bound paclitaxel / carboplatin in the treatment of lung squamous cell carcinoma of stage IIB and IIIA.

NCT ID: NCT01871805 Completed - Clinical trials for Non-Small Cell Lung Cancer

A Study of Alectinib (CH5424802/RO5424802) in Participants With Anaplastic Lymphoma Kinase (ALK)-Rearranged Non-Small Cell Lung Cancer (NSCLC)

Start date: September 30, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This non-randomized, open-label, multicenter study will evaluate the safety and efficacy of alectinib in participants with ALK-rearranged non-small cell lung cancer who failed crizotinib treatment. In Phase I, cohorts of participants will receive escalating doses of alectinib orally twice daily. In Phase II, patients who failed crizotinib treatment will receive the recommended phase II dose.