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Colon Cancer clinical trials

View clinical trials related to Colon Cancer.

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NCT ID: NCT01902953 Completed - Rectal Cancer Clinical Trials

Lymphoseek® as Lymphoid Tissue Targeting Agents in Colon Cancer(CNC)

Start date: March 2013
Phase: Phase 2
Study type: Interventional

45 patients undergoing a colon (large bowel/intestine)removal operation for the diagnosis of colon cancer will be included in this study. During colon operation the affected portion of the colon is removed. In addition, lymph nodes are included in the specimen and evaluated by a pathologist. Analysis of the lymph nodes in the specimen are important because this is an important aspect of determining the stage of the cancer. Once the standard technique is used for the colon removal operation and the specimen is removed it will be injected with two drugs to help identify the lymph nodes. One is a blue dye and the other a radiotracer. The colon and ALL of the lymph nodes will then be sent for the standard pathologic evaluation. The patient themselves will never be injected with these drugs being used for research. Following the standard lymph node evaluation, an additional pathologist at an outside research facility will further examine the lymph nodes in the specimen using more in depth techniques which are above and beyond the standard of care. The results of all the pathologic tests will be conveyed to the surgeon of record to help in their decision making regarding further treatment. The study hypothesis is that radiotracer will be at least as effective as blue dye in identifying the lymph nodes most likely to harbor cancer cells (sentinel nodes). Once identified, these sentinel nodes can then undergo a more in depth review leading to improved staging of colorectal cancer and more accurate treatment.

NCT ID: NCT01882972 Withdrawn - Colon Cancer Clinical Trials

Strength for Health

Start date: June 2013
Phase: N/A
Study type: Interventional

Despite a robust literature on the benefits of exercise for cancer survivors, most of the research to date falls in two primary areas - aerobic exercise and breast cancer survivors. The focus on aerobic training alone is a concern as resistance training is critical for building the muscle mass necessary to maintain physical function. However, concerns have been raised about the potential for higher than tolerated adverse event rates during resistance training, particularly that which is unsupervised, despite a history of safe use of resistance training in other chronically diseased patient populations. The aim of this pilot study is to demonstrate the feasibility, safety and quality of life benefit of a home-based resistance-training program among colorectal cancer survivors. The investigators will recruit n=30 men and women with stage I-III colon cancer. Participants will be randomized to a home-based exercise intervention that combines aerobic and resistance exercise. Control arm participants will receive a home-based meditation program.

NCT ID: NCT01882660 Terminated - Colon Cancer Clinical Trials

Pre-operative Decitabine in Colon Cancer: a Proof of Principle Study

DECO
Start date: July 2013
Phase: N/A
Study type: Interventional

Background of the study: Colon cancer is the second leading cause of cancer-related death world wide. Although patients presenting with early disease (stage I-III) can be cured, prognosis varies from 90% in stage I to 50-80% in stage II and III. Therefore, prevention of metastases after early disease is of utmost importance. Derepression of Wnt targets may provide a novel target for therapy. Objectives: The primary objective of the study is to assess in patients with primary colon cancer whether short-course pre-operative treatment with decitabine can increase Wnt target gene expression as measured in resected tumors compared to pretreatment biopsies. The secondary objective of the study is to assess in patients with primary colon cancer whether short-course pre-operative treatment with decitabine can revert CpG methylation and induce more favorable tumor characteristics as measured in resected tumors compared to pretreatment biopsies. The tertiary objective is to compare changes in Wnt target gene expression, CpG methylation and tumor characteristics for Wnt methylated and nonmethylated tumors as measured in resected tumors compared to pretreatment biopsies and identify new stratification markers.

NCT ID: NCT01868971 Completed - Colorectal Cancer Clinical Trials

Clinical Study to Establish the Feasibility and Usability of the EndoRingsā„¢

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this prospective clinical study is to establish the feasibility and usability of the ENDORINGSā„¢ when used during standard colonoscopy procedure.

NCT ID: NCT01855607 Terminated - Breast Cancer Clinical Trials

Topical Menthol for the Treatment of Chemotherapy Induced Peripheral Neuropathy

Start date: August 2013
Phase: Phase 2
Study type: Interventional

Primary Objective: To assess whether six-week treatment with twice daily topical Menthol application will decrease neuropathic pain as measured by the change in Brief Pain Inventory-Short Form (BPI-SF worst pain score), following or during neoadjuvant/adjuvant chemotherapy with taxane or platinum-based regimens among breast, gastrointestinal or gynecologic cancer patients. Secondary objectives: - To compare change in patient-reported outcomes: overall BPI-SF scales, EORTC-CIPN20, European Organization for Research and Treatment of Cancer Chemotherapy Quality of Life Questionnaire (EORTC QLQ-C30), Patient-Reported Outcomes Measurement Information System (PROMIS-29) scores between study groups. - To compare changes in dose delivery and early treatment discontinuation rates between study groups. - To compare objective sensory and motor functional change from baseline with the use of quantitative neurosensory testing. - To perform an exploratory analysis evaluating the interaction between treatment and chemotherapy type.

NCT ID: NCT01838109 Completed - Pancreatic Cancer Clinical Trials

Postoperative Oral Nutritional Supplementation After Major Gastrointestinal Surgery

Start date: April 2013
Phase: N/A
Study type: Interventional

Patients who underwent major gastrointestinal surgery is potentially at risk of malnutrition due to reduced oral intake, increased nutritional need, reduced gastrointestinal absorption function, and/or metabolic changes after surgery. The postoperative malnutrition is associated with low quality of life and seems to be related long-term nutritional status. This study is a multicenter, open-labeled prospective randomized clinical trial to examine the effect of postoperative oral nutritional supplements (ONS) after major gastrointestinal surgery by comparing the change of body weight and other nutritional parameters between the experiment group that is supplied with ONS and the control group without ONS.

NCT ID: NCT01801852 Recruiting - Breast Cancer Clinical Trials

Autologous Natural Killer T Cells Infusion for the Treatment of Cancer

Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and effectiveness of natural killer T (NKT) cell-based autologous adoptive immunotherapy in subjects with metastatic, treatment-refractory breast cancer, glioma, hepatocellular carcinoma, squamous cell lung cancer, pancreatic cancer, colon cancer or prostate cancer.

NCT ID: NCT01801059 Completed - Rectal Cancer Clinical Trials

Patient Activation Intervention in Improving Screening Rates for Colorectal Cancer

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

This randomized clinical trial focused on activating the patient to ask their health care provider for a colorectal cancer screening test to improve screening rates for colorectal cancer. The patient activation intervention may increase information seeking, number of screening tests ordered and number of completed screening tests for colorectal cancer.

NCT ID: NCT01797770 Recruiting - Rectal Cancer Clinical Trials

Trial on Mechanical Bowel Preparation in Laparoscopic Colorectal Surgery

MBP
Start date: January 2012
Phase: Phase 4
Study type: Observational

This is a Randomized trial on Mechanical Bowel Preparation in Laparoscopic Colorectal Surgery. In this trial patients with left sided colon and rectal tumors were randomized to receive mechanical bowel preparation or no preparation to assess postoperative complications and outcome

NCT ID: NCT01789983 Completed - Breast Cancer Clinical Trials

Feasibility of an Evidence-based Walking Program in Cancer Pts 60+ During Chemotherapy

WWE
Start date: October 2012
Phase:
Study type: Observational

The study will look at conducting a medium-intense walking program called Walk With Ease with cancer patients age 60 and above who are starting chemotherapy treatment. We will measure how many of these patients complete their participation in this program.