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Rectal Neoplasms clinical trials

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NCT ID: NCT00682786 Completed - Rectal Carcinoma Clinical Trials

Genotype-directed Neoadjuvant Chemoradiation for Rectal Carcinoma

Start date: October 2002
Phase: Phase 2
Study type: Interventional

Determine if genotype-directed neoadjuvant chemoradiation, using information from the thymidylate synthase promoter polymorphism, result in a greater degree of tumor downstaging in high risk patients compared to historical controls.

NCT ID: NCT00677586 Completed - Clinical trials for Rectal Neoplasm With Metastasis to the Liver

Simultaneous Versus Staged Resection for Initially Resectable Synchronous Rectal Cancer Liver-limited Metastasis

Start date: July 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of simultaneous liver resections compared to staged hepatectomies of rectal cancer with liver metastasis and to compare the short and long-term survival between the two groups.

NCT ID: NCT00671645 Terminated - Rectal Cancer Clinical Trials

Preoperative Combined RadioChemo-Molecular Target Therapy With Capecitabine, Bevacizumab, and Radiotherapy

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

- feasibility and tolerance of preoperative therapy with Bevacizumab in combination with Capecitabine and radiotherapy for patients with locally advanced, locally operable rectal carcinoma - collection of response rate (T- and M-downstaging, pathological complete remission)

NCT ID: NCT00663819 Terminated - Ulcerative Colitis Clinical Trials

Bioabsorbable Staple Line Reinforcement in Colorectal,Coloanal and Ileoanal Anastomoses

Start date: April 2008
Phase: N/A
Study type: Interventional

The primary purpose of this prospective, randomized multicenter center study is to evaluate and compare the outcomes of colorectal, coloanal and ileoanal anastomoses reinforced with a bioabsorbable staple line reinforcement material compared with standard non-reinforced colorectal, coloanal and ileoanal techniques with respect to the incidence of postoperative anastomotic leakage, anastomotic stricture and time to ileostomy closure, if applicable.

NCT ID: NCT00651677 Withdrawn - Rectal Cancer Clinical Trials

Hand Assisted Versus "Pure" Laparoscopic Assisted Proctectomy for Rectal Cancer

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

We hypothesize that hand-assisted laparoscopy will overcome technical difficulties related to pure laparoscopic rectal surgery and allow surgeons to expand application of laparoscopic techniques to treating patients with rectal cancer. In this study, we plan to randomly assign patients diagnosed with rectal cancer to undergo either "standard" laparoscopic surgery or hand-assisted laparoscopic surgery. We will then compare both peri-operative and long-term outcomes of patients.

NCT ID: NCT00648635 Active, not recruiting - Rectal Cancer Clinical Trials

Relationship Between Quality of Life, Treatment Modalities, and Patient Treatment/Outcome Expectations

Start date: March 12, 2008
Phase:
Study type: Observational

The goal of this study is to learn how the treatment given to patients with recurrent rectal cancer affects their well being and quality of life.

NCT ID: NCT00645710 Completed - Liver Metastases Clinical Trials

Hepatic Arterial Infusion of Floxuridine, Gemcitabine Hydrochloride, and Radiolabeled Monoclonal Antibody Therapy in Treating Liver Metastases in Patients With Metastatic Colorectal Cancer Previously Treated With Surgery

Start date: February 11, 2005
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as floxuridine and gemcitabine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Hepatic arterial infusion uses a catheter to carry cancer-killing substances directly into the liver. Radiolabeled monoclonal antibodies can find tumor cells and carry tumor-killing substances to them without harming normal cells. Giving hepatic arterial infusion of floxuridine together with gemcitabine hydrochloride and radiolabeled monoclonal antibody therapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase I/II trial is studying the side effects and best dose of floxuridine when given as a hepatic arterial infusion together with gemcitabine hydrochloride and radiolabeled monoclonal antibody therapy and to see how well it works in treating liver metastases in patients with metastatic colorectal cancer.

NCT ID: NCT00636948 Completed - Rectal Cancer Clinical Trials

Rectal Cancer Trial On Defunctioning Stoma

RECTODES
Start date: December 1999
Phase: N/A
Study type: Observational

The hypothesis of the present trial was that the use of a defunctioning loop stoma reduces the rate of symptomatic anastomotic leakage from 15% to 7.5% after low anterior resection of the rectum for cancer.

NCT ID: NCT00613080 Completed - Colorectal Cancer Clinical Trials

Combination Chemotherapy and Intensity-Modulated Radiation Therapy in Treating Patients Undergoing Surgery for Locally Advanced Rectal Cancer

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

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Giving these treatments before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving chemotherapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying the side effects and how well giving combination chemotherapy together with intensity-modulated radiation therapy works in treating patients undergoing surgery for locally advanced rectal cancer.

NCT ID: NCT00611858 Terminated - Rectal Cancer Clinical Trials

Cetuximab, 5-FU and Radiation as Neoadjuvant Therapy for Patients With Locally Advanced Rectal Cancer

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

The standard treatment for rectal cancer is to receive the chemotherapeutic drug 5-fluorouracil (5-FU) with radiation therapy before having surgery to remove the rectal cancer. This is known as neoadjuvant chemoradiotherapy. The purpose of this research study is to determine if Cetuximab improves the benefits of neoadjuvant chemoradiotherapy when given with 5-FU and radiation therapy.