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Colon Cancer clinical trials

View clinical trials related to Colon Cancer.

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NCT ID: NCT01582841 Completed - Colon Cancer Clinical Trials

Integrating Genetic Testing for Lynch Syndrome in a Managed Care Setting

HNPCC
Start date: February 2012
Phase: N/A
Study type: Interventional

The investigators research mobilizes the resources of an integrated health-delivery system with extensive electronic clinical data to implement and evaluate a new strategy to maximize screening of Colorectal Cancer (CRC) patients for Lynch Syndrome.

NCT ID: NCT01575990 Completed - Colon Cancer Clinical Trials

Elders Preferences in Care Decisions

EPIC-D
Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this research study is to explore ways to improve appropriate colorectal cancer (CRC) screening in the elderly by attempting to target screening in those most likely to benefit and avoiding screening in those least likely to benefit.

NCT ID: NCT01572428 Completed - Colon Cancer Clinical Trials

Narrow-Band Imaging Versus Standard White Light for the Detection of Serrated Lesions in the Proximal Colon

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

This is a study to determine if using Narrow-Band Imaging of the colon, rather than the usual white light on the colon, will improve the detection of a type of polyp called serrated. The polyps are called serrated because of their appearance under the microscope after they have been removed. They tend to be located up high in the colon, far away from the rectum. They have been definitely shown to be a type of precancerous polyp and it is possible that using Narrow-Band Imaging will make it easier to see them, as they can be quite difficult to see with standard white light.

NCT ID: NCT01569672 Completed - Breast Cancer Clinical Trials

Ohio Patient Navigator Research Program

OPNRP
Start date: November 2006
Phase: N/A
Study type: Interventional

The Ohio Patient Navigator Research Program (OPNRP) proposes to alleviate disparities in relation to the timely diagnosis and treatment of breast, cervical and colorectal cancer in Columbus, OH.

NCT ID: NCT01560377 Completed - Rectal Cancer Clinical Trials

Perfusion Assessment in Laparoscopic Left Anterior Resection

PILLAR II
Start date: May 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to demonstrate that NIR fluorescence angiography using the PINPOINT Endoscopic Fluorescence Imaging System ("PINPOINT System" or "PINPOINT") can assess viability of colon tissue during laparoscopic left colectomy. This information will provide the surgeon with clinically relevant information in assessing whether or not the tissue has adequate blood supply in the lower section of the colon prior to a colectomy.

NCT ID: NCT01558583 Completed - Prostate Cancer Clinical Trials

Online Study of Colorectal Cancer and Prostate Cancer Screening Decision Making

CARR2
Start date: July 2011
Phase: N/A
Study type: Interventional

Participants will be recruited from the United States and Australia to take an online survey about colon cancer screening or prostate cancer screening. Individuals selected for both the prostate cancer survey and the colon cancer study will be randomized to take one of three survey types - balance sheet, rating and ranking or conjoint analysis. These surveys will help participants clarify their values and opinions about screening options for colon cancer or prostate cancer. Participants' responses to the online survey are measured at one point in time - the time at which the participant takes the survey.

NCT ID: NCT01557881 Terminated - Lung Cancer Clinical Trials

Positron Emission Tomography/Magnetic Resonance Imaging in Patients

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

This clinical trial studies positron emission tomography (PET)/magnetic resonance imaging (MRI) in patients undergoing PET/computed tomography (CT). Diagnostic procedures, such as PET/MRI, may help doctors diagnose cancer or help doctors predict a patient's response to treatment

NCT ID: NCT01552226 Active, not recruiting - Rectal Cancer Clinical Trials

Compare Preperitoneal Analgesia to Epidural Analgesia for Pain Control After Colon and Rectal Surgery

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

This is a prospective randomized study of 114 patients. The purpose of this study is to compare the efficacy of two standard methods of analgesia for pain control in patients undergoing elective colon and rectal surgery, as measured by the Numeric Pain Scale (NPS) and by the need for supplemental narcotic analgesics. This study is designed to determine if postoperative pain control by local analgesics delivered through preperitoneally placed ON-Q Silver SoakerTM catheters (CPA) is equivalent to continuous epidural analgesia (CEA).

NCT ID: NCT01549535 Completed - Colon Cancer Clinical Trials

Polyp Detection With The Peerscope Systemâ„¢

Start date: February 2012
Phase: Phase 2
Study type: Interventional

The PeerScope System consists of Peer Medical camera heads, endoscopes, video system, light source and other ancillary equipment. The system is intended for endoscopic diagnosis, treatment and video observation of the digestive tract. The PeerScope system model B is indicated for use for endoscopy and endoscopic treatment within the lower digestive tract (including the anus, rectum, sigmoid colon, colon and ileocecal valve) of adults patients. Objective:To compare the additional diagnostic yield obtained by using the PeerScope Systemâ„¢ extended view vs. the diagnostic yield obtained by the Standard view colonoscopy. In addition, time measurements including time to cecum, time for withdrawal and overall procedure time will be analyzed and reported for each group.

NCT ID: NCT01547845 Completed - Breast Cancer Clinical Trials

Cancer Symptom Data From Multiple Treatment Centers

Start date: February 10, 2012
Phase:
Study type: Observational

Background: - Cancer and cancer treatments can cause symptoms and side effects. Pain, fatigue, and emotional distress are three common symptoms. Accurate reporting of these symptoms can improve treatment methods and outcomes. Even though symptom reporting is important to treatment, there is no method to collect and compare patient data from multiple cancer care centers. Researchers want to develop a method for collecting cancer patient symptom information from multiple centers. This method may help improve cancer treatment at hospitals and other care centers. Objectives: - To collect patient-reported symptom information from multiple cancer care centers. Eligibility: - Individuals at least 21 years of age who were treated for breast or colon cancer in the past year. - Participants will come from one of the participating cancer care centers. Design: - Participants will answer a short questionnaire about their symptoms during cancer treatment. Questions will ask about symptom severity and experiences. Other questions will ask how well the doctors and nurses managed the symptoms. - Participant responses will be compared with other medical and personal information. This information may include cancer type, age at diagnosis, and type of treatment. - Treatment will not be provided as part of this study.