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Colorectal Cancer clinical trials

View clinical trials related to Colorectal Cancer.

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NCT ID: NCT01879943 Terminated - Colorectal Cancer Clinical Trials

Capsule Versus Conventional Colonoscopy in Patient Following Colorectal Surgery

Start date: October 18, 2013
Phase: N/A
Study type: Interventional

The study will compare the diagnostic efficacy of the VCC (PillCam COLON 2) to standard colonoscopy in patients with prior colorectal surgery. The hypothesis is to validate the VCC as a means of screening for colonic polyps after resection, which would avoid a colonoscopy with its associated general anesthesia and potential side effects.

NCT ID: NCT01877096 Completed - Colorectal Cancer Clinical Trials

Motivational Interviewing for Colonoscopy

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

The purpose of this study is to begin to examine the efficacy of a motivational interviewing intervention to increase African Americans' screening colonoscopy rates. The results from this pilot study will allow us to estimate the magnitude of the intervention and mediation effect sizes.

NCT ID: NCT01874860 Completed - Colorectal Cancer Clinical Trials

Skin Rash Study Before Chemotherapy in Colorectal & Head and Neck Cancer Patients

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

The purpose of this study is to determine if using preventive treatments such as Doxycycline (an anti-biotic) capsules, sunscreen with SPF 30, Hydrocortisone 1% cream and a moisturizer will help to reduce the incidence and severity of the skin rash associated with Cetuximab (Erbitux®) when compared to receiving standard care for the treatment of skin rash.

NCT ID: NCT01871311 Terminated - Colorectal Cancer Clinical Trials

A Phase I Study of Nilontinib and Cetuximab in Patients With Solid Tumors

Start date: May 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the recommended Phase II dose of nilotinib when used in combination with cetuximab in the treatment of patients with recurrent and/or metastatic Kras wildtype colorectal cancer or squamous cell carcinoma of the head and neck.

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: NCT01862562 Active, not recruiting - Colorectal Cancer Clinical Trials

Trial to Evaluate Laparoscopic Versus Open Surgery in Elderly Colorectal Cancer Patients

Start date: August 2008
Phase: Phase 3
Study type: Interventional

Elderly patients have poorer preoperative conditions than younger patients. Therefore, minimally invasive surgery should be an effective treatment method for elderly patients. The investigators conducted a randomized trial that compared laparoscopic surgery and conventional open surgery in elderly patients who were 75 years old or over. The purpose of the present study was to clarify the effect of laparoscopic surgery in elderly patients. In our hypothesis of this trial, laparoscopic surgery is superior to conventional open surgery in short-term results, and same outcome in long -term results. Therefore, laparoscopic surgery would be recommended as standard procedure in an elderly colorectal patient.

NCT ID: NCT01856322 Terminated - Colorectal Cancer Clinical Trials

Surgery Plus Sulindac or Surgery Alone for Advanced Colorectal Cancer

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

Background: - Some types of inflammation may increase the risk of cancers in the intestinal track. Because of this possibility, anti-inflammatory drugs may be able to prevent tumor growth and spread. One such drug, sulindac, may be helpful to study. Researchers want to see if people who are having surgery to remove intestinal tumors from advanced colorectal cancer will benefit from sulindac. It will be tested against a placebo. Objectives: - To see if sulindac can improve treatment outcomes in people who are having surgery for advanced colorectal cancer. Eligibility: - Individuals at least 18 years of age who are having surgery for advanced colorectal cancer. Design: - Participants will be screened with a physical exam and medical history. Blood samples will be collected. Imaging studies and heart and lung function tests may also be given. - Participants will be separated into two groups. One group will take sulindac. The other will take a placebo. - Participants will take sulindac or placebo twice daily from about 2 to 3 weeks before the scheduled surgery. Seven days before the surgery, they will stop taking the pills. - Participants will have surgery to remove their tumors. The surgery will also remove affected organ tissue. - Participants will start to take the pills again once they have recovered from surgery. They will continue taking the sulindac or placebo twice a day for 3 years, or for as long as the tumors do not return.

NCT ID: NCT01853774 Completed - Colorectal Cancer Clinical Trials

Navigation From Community to Clinic to Promote CRC Screening in Underserved Populations

Start date: April 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to test the effectiveness of a two-phase intervention using "community-to-clinic navigators" to guide individuals from an especially hard-to-reach, multicultural, and underinsured population into primary care clinics and, subsequently, to track effects of the intervention on completion of colorectal cancer (CRC) screening in clinics. A cost-effectiveness analysis will lay the foundation for further implementation and dissemination research. Aim 1: Test effectiveness of community group education + tailored navigation versus community group education only in increasing clinic attendance among low-income, multicultural Arizona residents, aged 50 to 75 yrs. Hypothesis 1: Individuals receiving group education classes + tailored navigation will show higher rates of clinic attendance than those receiving only group education. * As a separate critical step for those who make clinic appointments, the investigators will examine the effect on follow through to screening, using initial group assignment as a control variable in analysis. Patients making clinic appointments will receive referral for screening and tailored navigation as usual care. Aim 2: Track outcomes of the Phase I intervention on CRC screening test completion among low-income, multicultural Arizona residents aged 50 to 75 years who attend clinic. Hypothesis 2: Individuals receiving group classes and tailored navigation during Phase I will have higher rates of CRC screening test completion than those receiving classes only, (however this outcome will be primarily due to clinic attendance). Aim 3: Determine the cost-effectiveness of each phase of the interventions on increasing CRC screening completion among low-income, multicultural Arizona residents aged 50 to 75 years. Exploratory Aim 4: Examine the levels of program dissemination from community to clinic to final screenings using the RE-AIM model. Research Question 2: What is the degree of Reach, Efficacy, Adoption, Implementation, and Maintenance of the community-to-clinic navigation, and clinic-to-screening outcomes?

NCT ID: NCT01850654 Completed - Colorectal Cancer Clinical Trials

Ohio Colorectal Cancer Prevention Initiative

OCCPI
Start date: December 26, 2012
Phase: N/A
Study type: Interventional

The purpose of the Ohio Colorectal Cancer Prevention Initiative (OCCPI) is to reduce morbidity and mortality due to colorectal cancer (CRC) in the state of Ohio. By identifying individuals at high-risk for CRC (genetically predisposed) and providing screening recommendations for cancer risk reduction, the OCCPI will understand how to increase length of life and quality of life for those diagnosed with CRC in Ohio, as well as to better prevent CRC in others in Ohio. Participants will have free tumor screening for Lynch syndrome, and may be eligible for free genetic testing and free genetic counseling as part of this study.

NCT ID: NCT01847599 Terminated - Colorectal Cancer Clinical Trials

Educational Intervention to Adherence of Patients Treated by Capecitabine +/- Lapatinib

ProMETheX
Start date: September 6, 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of the implementation of an educational program on adherence to capecitabine alone or in combination to lapatinib.