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Colorectal Cancer clinical trials

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NCT ID: NCT02804802 Recruiting - Colorectal Cancer Clinical Trials

Impact of DietarY and LIfestyle Risk Factors on Colorectal Cancer Screening

IDYLIC
Start date: February 2013
Phase: N/A
Study type: Observational

The main purpose of our project is to construct a lifestyle score based on a short questionnaire easy to complete and to validate it among participants in mass screening for colorectal cancer in Maine and Loire department over the next 2 years (2012 and 2013). We will evaluate the ability of our score to identify subjects with colorectal cancer diagnosed by the screening procedure (Hemoccult II ®, and colonoscopy if the test result is positive). Colorectal cancer will be the primary outcome for the assessment of the score's performance. The secondary endpoint will focus on colorectal adenomas diagnosed by the same procedure. Our secondary objectives are to test a second weighting system, evaluate the benefit in terms of predictive performance to add to the lifestyle score other dietary factors among that have a probable link with the risk of colorectal cancer, determine the acceptability of the questionnaire and to estimate by a cost-utility analysis the impact of applying a strategy of targeted screening using the developed score.

NCT ID: NCT02798224 Completed - Colorectal Cancer Clinical Trials

A Patient Portal Tool, E-assist, for Supporting CRC Screening

Start date: June 14, 2017
Phase: N/A
Study type: Interventional

To compare patient perceptions, intent to screen, and screening use among those using a patient portal with and without a colorectal cancer (CRC) screening decision support tool, e-assist. To evaluate whether the effectiveness of e-assist is moderated by multi-level factors, including patient health literacy, decision-making preference, and CRC screening decision stage. To assess program impact and create an implementation guide for e-assist by combining results from Aims 1 & 2, a program implementation analysis/process evaluation and the perspectives of staff from future diverse implementation sites including small primary care practices, University-based primary practices and federally-qualified health centers.

NCT ID: NCT02796820 Recruiting - Colorectal Cancer Clinical Trials

Huaier Granule As Adjuvant Therapy for Colorectal Cancer After Radical Surgery

Start date: June 2016
Phase: Phase 3
Study type: Interventional

A randomized, paralleled control clinical study investigating Huaier Granule for prevention of recurrence and metastasis of colorectal cancer after radical surgery, to evaluate the efficacy and safety.

NCT ID: NCT02792023 Recruiting - Colorectal Cancer Clinical Trials

Usefulness of Fecal Immunochemical Test in Iron Deficiency Anemia (IDAFIT)

IDAFIT
Start date: June 30, 2016
Phase: N/A
Study type: Interventional

Prospective study to test whether the immunochemical fecal occult blood test (FIT) for colorectal cancer (CRC) helps to prioritize patients with iron deficiency anemia for colonoscopy.

NCT ID: NCT02788955 Completed - Colorectal Cancer Clinical Trials

Protein Recommendation to Increase Muscle

PRIMe
Start date: April 2016
Phase: N/A
Study type: Interventional

This is a feasibility study to test the potential efficacy of diets of different amounts of protein and calories for patients with cancer. We hypothesize that nutritional deficits play a significant role in muscle loss and that nutritional therapy is an important first step in reversing or preventing muscle loss and maintaining/improving physical function.

NCT ID: NCT02788279 Completed - Colorectal Cancer Clinical Trials

A Study to Investigate Efficacy and Safety of Cobimetinib Plus Atezolizumab and Atezolizumab Monotherapy Versus Regorafenib in Participants With Metastatic Colorectal Adenocarcinoma (COTEZO IMblaze370)

Start date: July 5, 2016
Phase: Phase 3
Study type: Interventional

This is a Phase III, multicenter, open-label, three-arm, randomized study in participants with unresectable locally advanced or metastatic colorectal cancer (CRC) who have received at least two prior regimens of cytotoxic chemotherapy for metastatic disease. The study compares regorafenib, a standard of care therapy in this setting, to cobimetinib plus atezolizumab and atezolizumab monotherapy.

NCT ID: NCT02786329 Recruiting - Colorectal Cancer Clinical Trials

Anesthesia and Postoperative Outcome in Colorectal Cancer Patients

Start date: June 2016
Phase: Early Phase 1
Study type: Interventional

Study aims to compare the influence of TIVA and sevoflurane anesthesia with or without lidocaine on postoperative short and long term outcome in patients with colorectal cancer undergoing surgery. As short term endpoints postoperative pain and opioid consumption, resumption of bowel function, PONV, LOS will be registered. Long term outcome parameters include: the incidence of chronic pain, 1 and 5 years cancer recurrences incidence and mortality.

NCT ID: NCT02785146 Recruiting - Colorectal Cancer Clinical Trials

Adjuvant Chemotherapy Combined With Huaier Granule for Treating High-risk Stage II, Stage III Colorectal Cancer

Start date: June 2016
Phase: Phase 3
Study type: Interventional

A randomized, paralleled control clinical study investigating Huaier Granule for prevention of recurrence and metastasis of colorectal cancer after radical surgery, to evaluate the efficacy and safety.

NCT ID: NCT02785068 Withdrawn - Colorectal Cancer Clinical Trials

Evaluation of MM-151 + Nal-IRI + 5-FU + Leucovorin in RAS/RAF Wild-type Metastatic Colorectal Cancer

Start date: July 2016
Phase: Phase 1/Phase 2
Study type: Interventional

A phase 1b/2a study evaluating the combination of MM-151 + nal-IRI + 5-FU + Leucovorin in RAS/RAF wild-type Metastatic Colorectal Cancer.

NCT ID: NCT02784639 Completed - Colorectal Cancer Clinical Trials

Comparison of KRAS/BRAF Mutational Status With Conventional Techniques and Plasma Samples Analysis

KPLEX2
Start date: October 2013
Phase: N/A
Study type: Interventional

The goal of this multicenter prospective study is to validate, and ultimately translate in routine clinical practice, the use of plasma analysis of ccfDNA for the determination of KRAS mutation status in mCRC patients.