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Adenocarcinoma clinical trials

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NCT ID: NCT01367275 Terminated - Colorectal Cancer Clinical Trials

Irinotecan Plus Brivanib in Metastatic Colorectal Cancer (CRC) Enriched for Elevated Levels of Plasma FGF

Start date: August 2011
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if adding brivanib to irinotecan can help control the disease in patients with colorectal cancer that has spread. The safety of this drug combination will also be studied.

NCT ID: NCT01365156 Completed - Cervical Cancer Clinical Trials

Extraperitoneal Para-aortic Lymph Node Dissection (EPLND) for Cervix

Start date: August 2011
Phase: Phase 3
Study type: Interventional

The goal of this clinical research study is to learn if a surgical procedure called an extraperitoneal laparoscopic lymphadenectomy followed by chemotherapy and tailored radiation therapy can help to control the disease for a longer time than standard-of-care chemotherapy and whole pelvic radiation therapy.

NCT ID: NCT01365143 Terminated - Prostatic Neoplasms Clinical Trials

Prospective Randomized Trial Comparing Robotic Versus Open Radical Prostatectomy

Start date: May 2011
Phase: Phase 4
Study type: Interventional

To date, no study has prospectively compared open versus robotic radical prostatectomy in a randomized fashion for patients with prostate cancer. For patients with newly diagnosed prostate cancer who choose surgical management, the choice of surgical approach is often limited to surgeon preference and experience. This study will prospectively randomize patients with localized prostate cancer who are candidates for surgical management to open versus robotic radical prostatectomy.

NCT ID: NCT01363557 Terminated - Brain Metastasis Clinical Trials

Assess the Efficacy of Whole Brain Radiation Therapy in Lung Cancer Patients With Brain Metastasis

ARPEGE
Start date: March 2012
Phase: N/A
Study type: Interventional

Multicentre randomised (1:1) trial assessing the efficacy of whole brain radiotherapy in addition to Gefitinib for the management of brain metastasis in lung cancer patients with a mutated EGFR.

NCT ID: NCT01363466 Terminated - Clinical trials for Squamous Cell Carcinoma

Evaluation of Hysterectomy After Chemoradiation Therapy for Stage IB2/II Cervical Cancer

Start date: May 2003
Phase: Phase 3
Study type: Interventional

GYNECO 02 hypothesis is that hysterectomy reduces the possibility of local or loco-regional relapse, especially in patient with a reduced metastatic risk and who received a local chemoradiation therapy with an increase of radiotherapy doses (45 grays).

NCT ID: NCT01362790 Completed - Clinical trials for Pancreatic Neoplasms

SS1P and Pentostatin Plus Cyclophosphamide for Mesothelioma

Start date: May 11, 2011
Phase: Phase 1/Phase 2
Study type: Interventional

Background: - Malignant mesothelioma is a form of cancer that develops on the protective lining that covers the body's internal organs. It most often occurs on the lining of the lungs and chest wall or the lining of the abdomen. There is no known cure for malignant mesothelioma, so researchers are searching for new ways to treat it. - Mesothelin is a protein that is found in mesothelioma and other types of cancer cells. An experimental cancer drug called SS1P is designed to attack cells that have mesothelin while leaving healthy cells alone. Researchers want to test how effective SS1P is when it is given with pentostatin and cyclophosphamide. These drugs help suppress the immune system and may make the SS1P more effective. Objectives: - To study the effectiveness of SS1P plus two drugs that suppress the immune system to treat malignant mesothelioma. Eligibility: - Individuals at least 18 years of age who have malignant mesothelioma in the chest or abdomen. Design: - Participants will be screened with a physical exam, medical history, and blood tests. They will also have imaging studies. - The first treatment cycle will last 30 days. Up to three 21-day cycles of treatment will follow. - In the first cycle, participants will have pentostatin on days 1, 5, and 9. They will have cyclophosphamide on days 1 through 12. They will have SS1P on days 10, 12, and 14. - On the next three cycles, participants will have pentostatin on day 1.They will have cyclophosphamide on days 1 through 4. They will have SS1P on days 2, 4, and 6. - Participants will have frequent blood tests and other studies. They will receive all four cycles of treatment as long as there are no severe side effects. - Participants will have regular followup visits as directed by the study doctors.

NCT ID: NCT01362127 Completed - Clinical trials for Carcinoma, Squamous Cell

Neoadjuvant Chemotherapy Versus Radiochemotherapy for Cancer of the Esophagus or Cardia

NeoRes
Start date: October 2006
Phase: Phase 2
Study type: Interventional

The purpose of this randomized study is to clarify if neoadjuvant radiochemotherapy gives a higher degree of complete histological response than neoadjuvant chemotherapy before surgery in patients undergoing treatment for cancer of the esophagus or cardia.

NCT ID: NCT01360853 Completed - Clinical trials for Metastatic Pancreatic Adenocarcinoma

Gemcitabine and ON 01910.Na in Previously Untreated Metastatic Pancreatic Cancer

ONTRAC
Start date: May 2011
Phase: Phase 3
Study type: Interventional

The question being asked in this study is: Will patients with advanced pancreatic cancer live significantly longer if they are treated with a combination of Gemcitabine and ON 01910.Na than if they are treated with Gemcitabine alone? There are two parts to this study. In the first part of the study, patients with metastatic pancreatic cancer who have received no prior chemotherapy for this disease will be assigned by chance either to the group that will be treated with both Gemcitabine and ON 01910.Na (about 100 patients will be in this group) or, to the group that will be treated with Gemcitabine only (about 50 patients will be in this group). How long patients survive in the 2 groups will be compared. If it looks like there is no difference between the groups, the study will stop. If it looks like patients in the group that were treated with both Gemcitabine and ON 01910.Na survive longer, the study will continue into a second part where more patients will be treated in order to confirm and better understand the findings of the first part of the study.

NCT ID: NCT01360593 Completed - Pancreatic Cancer Clinical Trials

Gemcitabine/Capecitabine Followed by SBRT in Pancreatic Adenocarcinoma

Start date: July 25, 2011
Phase: Phase 2
Study type: Interventional

The current study seeks to further investigate the impact of up-front systemic therapy in combination with fractionated SBRT for potentially resectable, locally-advanced pancreatic adenocarcinoma.

NCT ID: NCT01360086 Completed - Gastric Cancer Clinical Trials

Fluorouracil, Cisplatin, Leucovorin Calcium, and Cetuximab in Treating Patients With Adenocarcinoma of the Stomach or Gastroesophageal Junction

Start date: June 2011
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as fluorouracil, cisplatin, and leucovorin calcium, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving more than one drug (combination chemotherapy) together with cetuximab before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving these drugs after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying the side effects of giving fluorouracil, cisplatin, and leucovorin calcium together with cetuximab and to see how well they work in treating patients with adenocarcinoma of the stomach or gastroesophageal junction.