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Tumor clinical trials

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NCT ID: NCT01215500 Completed - Cancer Clinical Trials

Dose Escalation of Hypofractionated Radiation Therapy in Patients With Metastatic Cancer

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

Patients with metastatic cancer are generally treated with chemotherapy, which has improved median survival compared to best supportive care. Despite this, patients continue to have persistent disease at sites that were initially involved with cancer. Radiation therapy is an effective modality for treating localized cancer but generally has been only used for palliation of symptoms once a patient develops metastatic disease. Since patients often have persistent disease after chemotherapy, the goal of this trial is to use increasing doses of radiation therapy to all sites of involved disease in order to determine the safety and efficacy of hypofractionated radiation therapy. The purpose of this study is to establish a maximum tolerated dose, dose-limiting toxicities, and recommended phase 2 dose of hypofractionated radiation therapy.

NCT ID: NCT01201018 Completed - Cancer Clinical Trials

Evaluation of the Safety and Efficacy of Oshadi D and Oshadi R for Cancer Treatment

Start date: January 2011
Phase: Phase 1
Study type: Interventional

The study will be non randomized, open label, dose rising study in cancer patients. Cancer treatment is consisting of 2 different drugs: Oshadi D and Oshadi R that will be administered orally. The study will include two sessions: - A single dose period to evaluate acute toxicity of each drug - Consecutive multiple increment dose escalation period of both drugs to determine the long-term safety, and the anticancer activity.

NCT ID: NCT01132014 Completed - Ovarian Cancer Clinical Trials

Autologous OC-DC Vaccine in Ovarian Cancer

Start date: May 2010
Phase: Early Phase 1
Study type: Interventional

This is a Five cohort sequential clinical trial for subjects with recurrent ovarian, fallopian tube, or primary peritoneal cancer to determine the feasibility and safety as well as immunogenicity of OC-DC, an autologous vaccine comprised of autologous dendritic cells (DC) loaded in vitro with lysate from autologous oxidized tumor cells, administered intranodally alone, or in combination with intravenous Bevacizumab and cyclophosphamide or in combination with intravenous Bevacizumab, cyclophosphamide and aspirin. Study duration is 24 months.

NCT ID: NCT01084460 Completed - Tumor Clinical Trials

Follow-up of the Natural Course of the Small EUS-suspected Gastric Gastointestinal Stromal Tumors

Start date: January 1997
Phase: N/A
Study type: Observational

Gastric gastrointestinal stromal tumors (GISTs) less than 2 cm are usually followed up conservatively. However, little is known about the natural course of small GISTs. The goal of this study was to evaluate the clinical course of the small EUS-suspected gastric GISTs and to determine the size predicting subsequent progression with increased malignant potential.

NCT ID: NCT00873145 Completed - Cancer Clinical Trials

Management of Bone Defects Around the Elbow

Start date: December 2008
Phase: N/A
Study type: Observational

Background: Bone defects of the distal humerus require complex reconstructions, for which standard prostheses may be insufficient. The researchers therefore investigated the clinical and radiological outcome of elbow reconstructions by megaprostheses.

NCT ID: NCT00861432 Completed - Tumor Clinical Trials

Evaluation of Questionnaires of Tumor Patients With and Without Additive Homeopathic Therapy

Start date: December 2008
Phase: Phase 2
Study type: Interventional

Tumor patients receiving conventional tumor therapies are included into this study. The patients are randomized into two groups receiving either additive homeopathic therapy or not. Two questionnaires referring to subjective feeling and life quality are filled out by the patients with each visit to the outpatients Department. One of them is the QLQC30 questionnaire of the EORTC. The results of the questionnaires of the two groups are compared.

NCT ID: NCT00806156 Completed - Ovarian Cancer Clinical Trials

Study to Evaluate the Safety and Efficacy of NKTR-102 in Patients With Metastatic or Locally Advanced Ovarian Cancer

Start date: October 2008
Phase: Phase 2
Study type: Interventional

This is a multicenter, open-label, two-arm, 2-stage, Phase 2 study of NKTR-102 in patients with metastatic or locally advanced platinum-resistant ovarian cancer. Approximately 70 patients will be randomized 1:1 into one of two treatment arms. NKTR-102 will be administered at a dose level of 145 mg/m^2 in both arms. In Arm A, NKTR-102 will be given on a q14d schedule. In Arm B, NKTR-102 will be given on a q21d schedule. After the initial 70 patients have been enrolled, Arm B will enroll approximately 110 additional patients.

NCT ID: NCT00802945 Completed - Breast Cancer Clinical Trials

Study to Evaluate the Safety and Efficacy of NKTR-102 in Patients With Metastatic or Locally Advanced Breast Cancer

Start date: October 2008
Phase: Phase 2
Study type: Interventional

This is a multicenter, open-label, two-arm, 2-stage, Phase 2 study of NKTR-102 in patients with metastatic or locally advanced breast cancer whose disease has failed prior taxane-based treatment in the metastatic setting. Patients will be randomized 1:1 into one of two treatment arms. NKTR 102 will be administered at a dose level of 145 mg/m2 in both arms. In Arm A, NKTR-102 will be given on a q14d schedule. In Arm B, NKTR-102 will be given on a q21d schedule. Approximately 70 patients may be evaluated in this study with approximately 35 patients enrolled in each treatment arm.

NCT ID: NCT00777751 Completed - Tumor Clinical Trials

Radiation Therapy and Cardiac Enzymes

Start date: October 6, 2008
Phase: N/A
Study type: Observational

The goal of this clinical research study is to learn if the radiation that you are receiving will result in an increase in certain proteins produced by the heart called cardiac biomarkers.

NCT ID: NCT00726128 Completed - Trauma Clinical Trials

Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System

VueLock
Start date: August 1998
Phase:
Study type: Observational

To prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System