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Colonic Neoplasms clinical trials

View clinical trials related to Colonic Neoplasms.

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NCT ID: NCT04196062 Completed - Colonic Neoplasms Clinical Trials

EndoMaster EASE System for Treatment of Colorectal Lesions

MASTERCESD
Start date: May 1, 2020
Phase: N/A
Study type: Interventional

This is a prospective, single arm study to assess the safety and performance of the EndoMaster EASE (Endoluminal Access Surgical Efficacy) System for the treatment of patients with colorectal neoplasms.

NCT ID: NCT04189393 Not yet recruiting - Colorectal Cancer Clinical Trials

Microbiome Analysis in esoPhageal, PancreatIc and Colorectal CaNcer Patients Undergoing Gastrointestinal Surgery

MA-PPING
Start date: January 1, 2020
Phase:
Study type: Observational

The MA-PPING is a multicenter prospective observational study that includes patients undergoing surgery for gastrointestinal cancer. The study aims to map the oral and gut microbiome of patients diagnosed with pancreatic, esophageal or colorectal cancer during their surgical patient journey from the moment of diagnosis until full recovery (three months after surgery).

NCT ID: NCT04188158 Recruiting - Clinical trials for Locally Advanced Colon Cancer

Analysis of the Effectiveness of Neoadjuvant Chemotherapy in the Treatment of Colon Cancer Locally Advanced (ELECLA)

ELECLA
Start date: March 10, 2017
Phase: Phase 2
Study type: Interventional

Effectiveness analysis of neoadjuvant chemotherapy in the treatment of locally advanced colon cancer. ELECLA trial

NCT ID: NCT04188002 Completed - Physical Activity Clinical Trials

A Web-based Tailored Health Behavior Intervention for Breast and Colon Cancer Survivors (eWellness)

eWellness
Start date: March 25, 2017
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare the differences in fruits and vegetable intake and physical activity from pre- to post- study between the intervention and control groups (i.e. the difference in differences). The study involves the use of web-based educational materials over a four week period. The investigators hypothesize that those in the intervention group will show a greater increase in fruit and vegetable intake and engage in more physical activity than those randomized to the control group. Eligible breast and colorectal cancer survivors from the UNC Health Registry/Cancer Survivorship Cohort (UNC HR/CSC) will be selected, consented, and randomized to either the intervention or control group. Both groups will fill out baseline surveys. The intervention group will receive a total to 4 newsletters for 4 weeks and at the beginning of week 5, they will asked to complete the follow-up survey online. The intervention newsletters focus on increasing physical activity and healthy diets. The control group will receive 4 newsletters in the same time frame as the intervention. The focus of the control group's newsletters will be on topics relevant to cancer survivors (e.g. getting back to work after treatment, managing finances) but will not focus on physical activity or diet. All contact with participants will take place online (i.e. surveys and newsletter delivery) from the study web site.

NCT ID: NCT04186117 Recruiting - Clinical trials for Metastatic Colon Cancer

Development of Clinical and Biological Database in Colorectal Cancer

CIRCUS
Start date: September 9, 2016
Phase: N/A
Study type: Interventional

Creation of circulating cancer cell-lines and caracterisation of these cell-lines which will be collected before any treatment in patients with metastatic colon adenocarcinoma

NCT ID: NCT04185272 Recruiting - Colonic Cancer Clinical Trials

Butyrophilins Role in Colon Cancer

Start date: June 30, 2020
Phase: N/A
Study type: Interventional

quantification of BTNL molecules in colon cancer in order to determinate if their could be used as a prognostic marquer

NCT ID: NCT04167436 Recruiting - Rectal Cancer Clinical Trials

Fit for Surgery. Multimodal Prehabilitation in Colorectal Cancer Patients

Start date: May 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

Randomized clinical trial of multimodal prehabilitation in vulnerable patients with colon or rectal cancer prior to surgery.

NCT ID: NCT04164069 Active, not recruiting - Pancreatic Cancer Clinical Trials

Dasatinib for the Prevention of Oxaliplatin-Induced Neuropathy in Patients With Metastatic Gastrointestinal Cancer Receiving FOLFOX Chemotherapy With or Without Bevacizumab

Start date: September 2, 2020
Phase: Phase 1
Study type: Interventional

This phase Ib trial studies side effects and best dose of dasatinib in preventing oxaliplatin-induced peripheral neuropathy in patients with gastrointestinal cancers who are receiving FOLFOX regimen with or without bevacizumab. Drugs used in chemotherapy, such as leucovorin, fluorouracil, and oxaliplatin (FOLFOX regimen), work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. However, the buildup of oxaliplatin in the cranial nerves can result in damage or the nerves. Dasatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Blocking these enzymes may reduce oxaliplatin-induced peripheral neuropathy.

NCT ID: NCT04160650 Completed - Cancer of Colon Clinical Trials

Educational Nursing Intervention Among Patients With Colorectal Cancer During Chemotherapy

Start date: October 21, 2019
Phase: N/A
Study type: Interventional

The prevalence of malnutrition is common among patients with colorectal cancer. Chemotherapy induced side effects may impact negatively on nutrition intake thus increase the risk of malnutrition and serious complications for patients. Purpose is to test the effect of empowering education on activation and knowledge level among patients with colorectal cancer during the chemotherapy. Secondary outcomes are quality of life and malnutrition. A two-arm, single center, patient blinded superiority trial with stratified randomization (1:1) and with repeated measures is used to measure the effectiveness of face-to-face education on nutrition intake related chemotherapy induced side-effects' self-care compared to standard care. Eligibility criteria are adult patients diagnosed with colorectal cancer and receiving intra venous chemotherapy treatment. Patients are recruited in one university hospital outpatient clinic in Finland. Experienced oncology nurse delivers the intervention two weeks after the first chemotherapy. Primary outcomes are activation in self-care and knowledge level. Secondary outcomes are quality of life and risk of malnutrition measured at baseline (M0) and after eight (M1) and 16 weeks (M2) after the intervention. The study will provide knowledge of nurse-led educational intervention on self-care among patients with colorectal cancer. The findings will contribute to patient education and self-care, thus better quality of life.

NCT ID: NCT04147481 Enrolling by invitation - Gastric Cancer Clinical Trials

Effects of Abdominal Nerve Block on Postoperative Recovery in Patients Undergoing Gastrointestinal Surgery

Start date: October 21, 2019
Phase: N/A
Study type: Interventional

To explore the effect of general anesthesia combined with transversus abdominis plane block (TAPB) and/or rectus sheath block (RSB) on the recovery of patients with gastrointestinal tumor after surgical treatment.