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Colorectal Cancer clinical trials

View clinical trials related to Colorectal Cancer.

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NCT ID: NCT01923155 Completed - Colorectal Cancer Clinical Trials

Safety & Effectiveness of Nurse Performed Colonoscopies Under Supervision

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

There is no theoretical or practical reason why non-medical personnel such as nurses could not be trained to perform diagnostic colonoscopy with comparable proficiency as medical endoscopists. Nurse endoscopists have been widely accepted in the United Kingdom for the past 15 years as a valuable resource to cope with the increasing demand for endoscopic service, in particular diagnostic colonoscopy for colorectal screening. A pilot study performed in Hong Kong in 2008 has shown that endoscopy nurses can be trained to perform diagnostic endoscopy safely and reliably. This study aims to demonstrate that properly trained nurse endoscopists have a comparable proficiency in performing colonoscopy procedures as their medical counterparts.

NCT ID: NCT01919151 Recruiting - Colorectal Cancer Clinical Trials

Micrometastasis in Gastrointestinal Cancer

Start date: June 2008
Phase: N/A
Study type: Observational

Prognostic and predictive value of assessing the patients micrometastasis status in blood and bone marrow when diagnosed GI cancer. 2 different patient subgroups are currently studied, patients with cancer of the pancreas and patients with liver metastasis secondary to colorectal cancer. Our hypothesis is that patients with detective circulating tumor cells in the blood or disseminated tumour cells in their bone marrow at diagnosis have a more advanced disease than negative patients. This information may be of therapeutic interest.

NCT ID: NCT01918852 Completed - Colorectal Cancer Clinical Trials

S-1 Versus Capecitabine in the First Line Treatment of MCC Patients.

SALTO
Start date: December 2013
Phase: Phase 3
Study type: Interventional

The study is a two-arm randomised phase III trial. Patients will be randomised to receive capecitabine (arm A) or S-1 (arm B). Bevacizumab may be added according to the choice of the investigator. Patients will be followed 3-weekly at the outpatient clinic, toxicity will be assessed according to study protocol guidelines. Patients will be evaluated every 3 cycles for response. Upon disease progression patients will be treated according to the local investigators

NCT ID: NCT01917513 Completed - Colorectal Cancer Clinical Trials

Prospective Trial to Compare the Clinical Efficiency of G-EYE™ HD Colonoscopy With Standard HD Colonoscopy

Start date: May 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the adenoma detection rate of G-EYE™ high definition colonoscopy with that of standard high definition colonoscopy

NCT ID: NCT01916239 Completed - Colorectal Cancer Clinical Trials

Pomegranate Extract Supplementation in Colorectal Cancer Patients

POMEcolon
Start date: June 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The most relevant pomegranate phenolics (ellagitannins and ellagic acid) are extensively metabolized by the human gut microbiota to yield a number of metabolites called urolithins (mainly Uro-A). Urolithins have been reported to regulate in vivo the expression of genes involved in inflammation and cancer. Our hypothesis is that urolithins can be detected in the human colon mucosa where these metabolites can exert anti-inflammatory and anti-cancer activities. After colonoscopy and diagnosis, colorectal cancer patients will consume capsules containing three different pomegranate extract formulations until surgery. The aims of this trial are: - To evaluate the disposition of pomegranate phenolics and urolithins in tumoral and normal colon tissues. - To evaluate gene expression profiling and protein markers in tumoral and normal colon tissues from these patients. - To compare different pomegranate extract formulations on the above.

NCT ID: NCT01911988 Active, not recruiting - Colorectal Cancer Clinical Trials

Study of Association Between Peripheral Immune Cells and Recurrence in Stage II/III Colorectal Cancer

PICC-1
Start date: June 2013
Phase: N/A
Study type: Observational

The purpose of this study is to determine association between Peripheral Immune Cells(PIC) and recurrence in stage II/III colorectal cancer

NCT ID: NCT01906008 Completed - Colorectal Cancer Clinical Trials

Phase II Study of Minocycline for Reducing Symptom Burden in Colorectal Patients

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

The goal of this clinical research study is to learn if minocycline can reduce numbness, pain, and/or loss of motor function in patients with colorectal cancer. In this study, minocycline will be compared to a placebo. The study doctor can explain how the study drug is designed to work. A placebo is not a drug. It looks like the study drug, but it is not designed to treat any disease or illness. It is designed to be compared with a study drug to learn if the study drug has any real effect.

NCT ID: NCT01904955 Completed - Colorectal Cancer Clinical Trials

Should Colorectal Cancer Patients be Followed After Five Years? Study of Recurrence in a Population Cohort

Start date: September 2010
Phase: N/A
Study type: Observational [Patient Registry]

The results of this study will make it possible, thanks to better understanding of the natural history of colorectal cancer, to define new treatment and surveillance strategies for colorectal cancers resected with curative intent, so as to improve management and thus improve patient survival. These data will also make it possible to calculate the prevalence of patients who require treatment or surveillance because of their disease.

NCT ID: NCT01904890 Completed - Colorectal Cancer Clinical Trials

AANCART Research Project on Lay Health Workers and Asian Americans

AANCARTLHW
Start date: March 2012
Phase: N/A
Study type: Interventional

This is a behavioral research study to evaluate the effectiveness of a type of health education, lay health worker (LHWs), on increasing the use of a routine health behavior, colorectal cancer (CRC) screening, among Asian Americans, who underutilize such screening. Using quantitative and qualitative methods and a community-based participatory research (CBPR) approach, the project will develop and implement a group randomized controlled trial to evaluate LHW effectiveness in promoting CRC screening among Asian Americans age 50 to 75. The investigators will conduct focus groups and individual interviews with community participants to revise training and survey materials developed in prior projects. The investigators will recruit LHWs to be randomly assigned to the intervention arm and to the comparison arm. The LHWs will each recruit 15 participants from their social network. Intervention LHWs will be taught to teach their participants about CRC screening through 2 outreach sessions and 2 telephone calls aimed at increasing their CRC screening receipt. LHWs and participants in the comparison group will receive a bilingual CRC brochure as well as 2 lectures on healthy nutrition for cardiovascular health delivered by a health educator and an optional post- intervention LHW outreach session on CRC screening. Effectiveness of the intervention will be measured by pre-intervention and post-intervention surveys of community participants' CRC screening behaviors. The investigators will also conduct ethnographic observations of LHWs and their participants during the small group sessions and post- intervention focus groups to understand how such a health education approach may work.

NCT ID: NCT01904630 Completed - Colorectal Cancer Clinical Trials

Sequencing to Identify Gene Variants in Familial Colorectal Cancer

Start date: December 2012
Phase: N/A
Study type: Observational

The project will use exome sequencing to search for genetic predispositions for familial colorectal cancer (CRC). Except for certain syndromes there is today no good method for identifying individuals with a hereditary high risk for CRC (about 25% of the cases). There is currently no routine screening of the population in Norway for CRC today. Coloscopy, which is the most reliable method, is demanding with respect to resources, it can be painful, and may have complications. This project will attempt to find genetic determinants for identification of individuals with increased risk for familial CRC. Such methods will reduce unnecessary medical examination of unaffected family members, and will make it easier to focus health services on individuals with increased risk. This will represent a significant contribution towards improved health reduced death rate caused by CRC. The project includes research on the ethical aspects, in particular challenges related to how feedback to donors is handled.