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Rectal Neoplasms clinical trials

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NCT ID: NCT00433576 Completed - Clinical trials for Adenocarcinoma of the Rectum

Resveratrol in Treating Patients With Colorectal Cancer That Can Be Removed By Surgery

Start date: December 2006
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and best dose of resveratrol in treating patients with colorectal cancer that can be removed by surgery. Resveratrol may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT00427375 Completed - Rectal Neoplasms Clinical Trials

Local Excision in Downstaged Rectal Cancer

GRECCAR 2
Start date: March 5, 2007
Phase: Phase 3
Study type: Interventional

Patients with T2T3 low rectal cancer (size =< 4 cm) received neoadjuvant treatment (50Gy in 5 weeks with concomitant chemotherapy. Good responders (residual tumour =< 2 cm) are randomised in local vs rectal excision, 6-8 weeks after treatment. The composite end point evaluates the rate of patients with death, recurrence, major morbidity or severe after effects at two years.

NCT ID: NCT00422864 Completed - Rectal Cancer Clinical Trials

A Single Arm Trial of Oxaliplatin and 5FU With Concurrent Radiation in Patients With Metastatic Rectal Cancer

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

This trial is a single-arm study for patients presenting with both local and metastatic adenocarcinoma of rectum. The aims of the trial are (1) to determine the tolerability rate, and (2) to determine toxicity rates, pelvic and distant response rates in patients with locally advanced rectal cancer in the presence of distant metastasis who are treated with an interdigitating chemotherapy (oxaliplatin/5-fluorouracil [5FU]) and radiotherapy regimen.

NCT ID: NCT00421824 Completed - Rectal Neoplasms Clinical Trials

Study of Neoadjuvant Chemotherapeutic Treatment (XELOX) Followed by Chemoradiotherapy (XELOX/RT) and Surgery Versus Chemoradiotherapy Followed by Surgery and Chemotherapy in Patients With High Risk Rectal Cancer

Start date: May 2006
Phase: Phase 2
Study type: Interventional

Primary: - To assess complete pathological response rate of both strategies. Secondary: - Safety profile - To assess downstaging rate of both strategies. - To compare relative dose intensity of oxaliplatin and capecitabine of both strategies - To compare time to progression and overall survival of both strategies.

NCT ID: NCT00414232 Completed - Rectal Cancer Clinical Trials

Prospective Assessment of Symptoms and Quality of Life in Rectal Cancer Patients Receiving Chemo-Radiotherapy

Start date: November 2006
Phase:
Study type: Observational

Prospective Assessment of Symptoms and Quality of Life in Rectal Cancer Patients Receiving Chemo-Radiotherapy.

NCT ID: NCT00409994 Completed - Rectum Cancer Clinical Trials

Safety Study of Rapamycin Administered Before and During Radiotherapy to Treat Rectum Cancer

Start date: September 2006
Phase: Phase 1/Phase 2
Study type: Interventional

Investigating the safety and the activity of Rapamycin, administered before and during preoperative radiotherapy in patients with an operable colorectal carcinoma. The phase I dose escalation study will be performed in three steps (2, 4 and 6 mg). Patients entered in phase II will follow the same tolerable treatment regimen as patients in phase I study.

NCT ID: NCT00407654 Completed - Clinical trials for Recurrent Rectal Cancer

VEGF Trap in Treating Patients With Previously Treated Metastatic Colorectal Cancer

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

This phase II trial is studying how well VEGF Trap works in treating patients with previously treated metastatic colorectal cancer. VEGF Trap may stop the growth of colorectal cancer by blocking blood flow to the tumor.

NCT ID: NCT00403624 Completed - Rectal Neoplasms Clinical Trials

Evaluation of the Neoadjuvant Treatment With Oxaliplatin -UFT- Radiotherapy in Rectal Cancer

Start date: July 2001
Phase: Phase 1/Phase 2
Study type: Interventional

Primary objective: - To evaluate the rate of responses to neoadjuvant therapy + radiotherapy Secondary objective: - tolerability (toxicity) and time to progression

NCT ID: NCT00397878 Terminated - Clinical trials for Recurrent Rectal Cancer

AZD0530 (NSC 735464) in Treating Patients With Previously Treated Metastatic Colon Cancer or Rectal Cancer

Start date: November 2006
Phase: Phase 2
Study type: Interventional

This phase II trial is studying how well AZD0530 works in treating patients with previously treated metastatic colon cancer or rectal cancer. AZD0530 may stop the growth of tumor cells by blocking blood flow to the tumor and by blocking some of the enzymes needed for cell growth.

NCT ID: NCT00397384 Completed - Clinical trials for Stage IV Non-small Cell Lung Cancer

Erlotinib Hydrochloride and Cetuximab in Treating Patients With Advanced Gastrointestinal Cancer, Head and Neck Cancer, Non-Small Cell Lung Cancer, or Colorectal Cancer

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

This phase I trial is studying the side effects and best dose of erlotinib hydrochloride when given together with cetuximab and to see how well they work in treating patients with advanced gastrointestinal cancer, head and neck cancer, non-small cell lung cancer, or colorectal cancer. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. 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. Erlotinib hydrochloride and cetuximab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving erlotinib hydrochloride together with cetuximab may kill more tumor cells.