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Tumor clinical trials

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NCT ID: NCT01182779 Recruiting - Tumor Clinical Trials

Trial of Proton Versus Carbon Ion Radiation Therapy in Patients With Chordoma of the Skull Base

HIT-1
Start date: July 2010
Phase: Phase 3
Study type: Interventional

This study is a prospective randomised clinical phase III trial. The primary objective of this study is to evaluate, if the innovative therapy (carbon ion irradiation) in chordomas is superior to the standard proton treatment with respect to the local-progression free survival (LPFS).

NCT ID: NCT01105520 Recruiting - Tumor Clinical Trials

Neurologic and Neurophysiologic Assessment of Clinical Course in Patients With Intraspinal Processes

Start date: January 2010
Phase: Phase 1
Study type: Observational

Patients included in the study are treated at the Klinik für Neurochirurgie USZ. The clinical course is documented at Paraplegikerzentrum Balgrist using validated diagnostic procedures (e.g. SCIM, ASIA, neurophysiology). Study aims: Prognostic value of clinical diagnosis and additional diagnostic procedures? Which parameters exhibit optimal prognostic power? Differences between tumor/AVM associated lesions and traumatic lesions? What can we learn for pathophysiology and treatment? - Trial with surgical intervention

NCT ID: NCT01093079 Recruiting - Tumor Clinical Trials

Laparoscopic Versus Open Partial Nephrectomy - Surgical and Oncological Outcomes

LapVsOpen prtn
Start date: September 2009
Phase: N/A
Study type: Observational

Partial Nephrectomy is the standard care for small (<4 cm) renal tumors. Despite the expanding use of laparoscopic approach, debate exist regarding the short and long term outcomes compared to the open approach. Our goal is to perform a prospective randomized trial to compare these methods

NCT ID: NCT00979277 Recruiting - Cancer Clinical Trials

Transcriptomal and Molecular Characterization of Tumor Associated Monocytes/Macrophages in Human Cancers

Start date: n/a
Phase: N/A
Study type: Observational

Recent studies from both human and mice cancer models have demonstrated a crucial role for monocytes/macrophages in contributing to cancer progression and disease prognosis. However, since each cancer subtypes is associated with a unique tumor microenvironment in terms of its anatomical location, cytokine/chemokine profiles and stromal components, the functional contribution of tumor infiltrating cells such as the monocytes/macrophages can be equally diverse, depending on the type of cancer. Therefore to obtain a global understanding of the role of host immune cells in cancer progression, it is necessary to accurately characterize these cells in the context of the tumor microenvironment for several cancer subtypes rather than a single cancer. In view of this, this pilot proposal aims to carryout a systems approach in characterizing the functional phenotype of monocyte/macrophage lineage in 4 diverse human cancer types [e.g., Colorectal Cancer, Nasopharyngeal carcinoma, Hepatocellular (liver) cancer and Renal cell carcinoma (kidney cancer)] and the molecular basis of tumor-induced immunosuppression in each of these conditions. Besides providing a global view of the host innate immunity and its molecular basis in these human cancer, the outcome of this investigation will be crucial in defining the scopes of specific immunotherapy strategies to overcome tumor-induced immunosuppression and induce monocyte/macrophage-mediated antitumor response.

NCT ID: NCT00690261 Recruiting - Lung Cancer Clinical Trials

The Impact of M1/M2 Tumor Associated Macrophage (TAM) Polarization on Cancer Progression and Prognosis Prediction

Start date: September 2007
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the correlation between M1/M2 phenotype of tumor associated macrophage (TAM) in lung cancer patients and clinical outcome.

NCT ID: NCT00633490 Recruiting - Tumor Clinical Trials

Study of Apatinib as an Inhibitor of Tumor Angiogenesis

Start date: July 2007
Phase: Phase 1
Study type: Interventional

Apatinib is a tyrosin-inhibitor agent targeting at vascular endothelial growth factor receptor (VEGFR), so it can inhibit tumor angiogenesis. This phase I study aims to determine the drug's toxicity and to find a dose level to be used in a phase II study in solid tumor patients.