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Colonic Neoplasms clinical trials

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NCT ID: NCT03084809 Completed - Colorectal Cancer Clinical Trials

Chemotherapy Combined With CIK Treating Colon Cancer

Start date: May 6, 2012
Phase: Phase 4
Study type: Interventional

Cytokine-induced killer cells (CIK) is an auxiliary antitumor treatment. The investigators aim to evaluate the clinical efficacy of chemotherapy combined with CIK in the treatment of postoperative colorectal cancer patients. And to provide useful reference for the clinical application of CIK in colorectal cancer patients.

NCT ID: NCT03072641 Completed - Colon Cancer Clinical Trials

Using Probiotics to Reactivate Tumor Suppressor Genes in Colon Cancer

Start date: June 3, 2010
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if probiotic bacteria have a beneficial effect on the colon cancer-associated microbiota and epigenetic alterations in colon cancer. Dietary supplementation consists of two ProBion Clinica tablets, yielding a daily dose of 1.4 x 10 ˄ 10 Bifidobacterium lactis Bl-04 (ATCC SD5219), 7x10 ˄ 9 Lactobacillus acidophilus NCFM (ATCC 700396), and 0.63 g inulin.

NCT ID: NCT03072095 Completed - Cancer of the Colon Clinical Trials

Colorectal Cancer Screening in a Community Health Setting

Start date: April 17, 2017
Phase: N/A
Study type: Interventional

This randomized controlled pilot study at the Health Annex, Family Practice & Counseling Network (FPCN), a community clinic in Southwest Philadelphia, aimed at providing data on the feasibility of a mailed FIT approach to CRC screening in a community health setting, and how patients respond to text messaging and behavioral economic engagement incentives.

NCT ID: NCT03068052 Completed - Cancer of the Colon Clinical Trials

Behavioral Economic Incentives and Cancer Health Risk Assessment

Start date: May 8, 2017
Phase: N/A
Study type: Interventional

This is an RCT among UPHS employees between ages 50-64 comparing no incentive and a loss-framed incentive for completing cancer health risk assessment. Those eligible will receive the phone number for direct colonoscopy scheduling, with the incentive arm receiving an additional unconditional incentive. The primary outcome is completion of screening colonoscopy. Secondary outcomes include scheduling of colonoscopy and completion of risk assessment.

NCT ID: NCT03037385 Completed - Neoplasms Clinical Trials

Phase 1/2 Study of the Highly-selective RET Inhibitor, Pralsetinib (BLU-667), in Participants With Thyroid Cancer, Non-Small Cell Lung Cancer, and Other Advanced Solid Tumors

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Start date: March 17, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase 1/2, open-label, first-in-human (FIH) study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antineoplastic activity of pralsetinib (BLU-667) administered orally in participants with medullary thyroid cancer (MTC), RET-altered NSCLC and other RET-altered solid tumors.

NCT ID: NCT03035136 Completed - ColoRectal Cancer Clinical Trials

Retrospective Study on Epidemiology of Colorectal Lesions

Start date: January 15, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Retrospective analysis on colonoscopies in the endoscopy unit of the Lyell McEwin Hospital.

NCT ID: NCT03031171 Completed - ColoRectal Cancer Clinical Trials

Community Engaged Colon Cancer Screening Patient Navigator Program

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

The goal of the project is to increase colorectal cancer screening within the priority population of female and male adults age 50 to 85 in Northern Nevada. A successful community-based cancer patient navigator program will be modified in partnership with the community into a multi-level screening intervention.

NCT ID: NCT03028831 Completed - Colon Cancer Clinical Trials

Fiber to Reduce Colon Cancer in Alaska Native People

Start date: December 11, 2017
Phase: N/A
Study type: Interventional

Alaska native people (AN) have the highest recorded incidence and death rate from colon cancer in the world (>90:100,000). We hypothesize that the AN, despite their high consumption of anti-inflammatory and antineoplastic n-3 fish oils, are at increased risk of colon cancer because of colonic butyrate deficiency resulting from their remarkably low consumption of fiber-containing foods. We hypothesize that fiber supplementation of their usual diet will result in a bloom of butyrate producing microbes in the colon, resulting in increased butyrate production, which will suppress their high microbial secondary bile acid production, antagonize the actions of other food (smoked fish) and environmental carcinogens (tobacco, alcohol), and interact with the high circulating levels of n-3 fish oils to suppress colonic inflammation and cancer risk. In order to investigate this, we will conduct a randomized double-blinded 4-week clinical trial in up to 100 randomizable healthy, middle-aged AN undergoing screening colonoscopy, with the objective of obtaining 60 completed interventions. The interventions will consist of either a high-dose soluble fiber supplement given as a drink, together with their usual diet which currently contains about 15g total fiber/d, or to a control digestible starch drink plus their usual diet. The primary endpoint will be a clinically significant reduction in Ki67 proliferative colonic mucosal biomarkers of cancer risk. Microbiome and metabolome mechanisms responsible for the anticipated changes in mucosal biomarkers will also be investigated. Our results in extreme risk AN will be further evaluated by comparison to similar measurements previously made in minimal risk rural Africans and intermediate risk African Americans. Our results will be used to provide the scientific basis for a definitive large-scale high-fiber supplementation study (to achieve >50g total fiber/d) to suppress adenomatous polyp recurrence following colonoscopy.

NCT ID: NCT03019016 Completed - Crohn Disease Clinical Trials

Comparison of Intracorporeal and Extracorporeal Anastomoses for Minimally Invasive Right Colectomy

Start date: August 2016
Phase: N/A
Study type: Observational

The primary objective of this study is to retrospectively compare the perioperative and short-term (discharge through 30 days) outcomes of intracorporeal and extracorporeal anastomosis in minimally invasive right colectomies for benign and malignant disease. The secondary objective of this study is to retrospectively compare the rates of incisional hernia (up to 6 month post procedure) between intracorporeal and extracorporeal arms.

NCT ID: NCT02955901 Completed - Colonic Neoplasms Clinical Trials

3-day vs. 1-day Low Residue Diet Influence in Colonoscopy Preparation and Patient Tolerability

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Colonoscopy is one of the most common methods for the diagnosis and treatment of lower gastrointestinal tract diseases and provides a unique opportunity to identify early neoplastic lesions. Adequate bowel preparation is important for optimal colonoscopy. New bowel-cleansing regimens, study of patient-related risk factors to fail a proper preparation and diet adaptations have been studied recently. A low residue diet is the standard in the day before the colonoscopy. Some endoscopists prescribe this dietary plan for a 3-day period prior to the exam, although no study compared the recommended 1-day versus 3-day diet regime, or the influence in bowel preparation results. The aim of this project is to determine if the use of a 3-day low residue diet improves bowel preparations results and the influence in patient tolerability and adherence.