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Colorectal Neoplasms clinical trials

View clinical trials related to Colorectal Neoplasms.

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NCT ID: NCT01955837 Completed - Colorectal Cancer Clinical Trials

Study of Trifluridine/Tipiracil (TAS-102) in Patients With Metastatic Colorectal Cancer in Asia

TERRA
Start date: September 2013
Phase: Phase 3
Study type: Interventional

To compare the effects of TAS-102 with placebo in patients with metastatic colorectal cancer refractory or intolerable to standard chemotherapies.

NCT ID: NCT01955629 Completed - Clinical trials for Colorectal Cancer Metastatic

Study of Aflibercept as Maintenance Therapy Following Induction With Aflibercept in Combination With XELOX, as First-Line Treatment for Metastatic Colorectal Cancer Patient

AMOR
Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Primary Objectives: Study Part 1: To determine the recommended dose for the aflibercept, oxaliplatin and capecitabine (XELOX) combination to be used in the Part 2 of the study. Study Part 2: To assess the percentage of patients without progression of the disease at 6 months after the start of maintenance therapy with aflibercept single-agent, following the first-line induction therapy with XELOX and aflibercept combination in patients with previously untreated metastatic colorectal cancer. Secondary Objective: Study Part 2: Include the evaluation of progression free survival, overall survival, response to treatment, the overall safety (during induction and maintenance therapy) and the assessment of aflibercept pharmacodynamics and biomarkers parameters.

NCT ID: NCT01950403 Completed - Colorectal Cancer Clinical Trials

Linaclotide Acetate in Preventing Colorectal Cancer in Healthy Volunteers

Start date: September 2013
Phase: Phase 1
Study type: Interventional

This randomized phase I trial studies the side effects and best dose of linaclotide acetate in preventing colorectal cancer in healthy volunteers. Chemoprevention is the use of certain drugs to keep cancer from forming. The use of linaclotide acetate may prevent colorectal cancer.

NCT ID: NCT01946711 Completed - Rhinosinusitis Clinical Trials

Buparid/PARI SINUS Versus Budes® Nasal Spray in the Therapy of Chronic Rhinosinusitis With Polyposis Nasi

Start date: August 28, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The study should create data for the selection of a clinically relevant primary endpoint to assess the efficacy and safety of Buparid/PARI SINUS as compared to Budes Nasal Spray in the therapy of chronic rhinosinusitis (CRS) with polyposis nasi in adult patients. Ideally, the selected parameter should allow a correlation between an objective methodology and the clinical outcome of the study patients.

NCT ID: NCT01946282 Completed - Colorectal Cancer Clinical Trials

Evidence-Based Colorectal Cancer Screening for the Uninsured

Start date: November 2013
Phase: N/A
Study type: Interventional

Through this program, the investigators will test a systematic colon cancer screening outreach strategy for increasing screening completion among uninsured patients, not up-to-date with screening. The intervention will consist of mailed screening invitations, with processes such as phone reminders to promote screening and evidence based follow up. All patients will be randomly assigned to receive mailed invitations to complete a home fecal immunochemical test (FIT). Some patients will be randomly assigned to receive a small financial incentive on completion of FIT testing.

NCT ID: NCT01944137 Completed - Breast Cancer Clinical Trials

Improving Care After Chemotherapy

IMPACT
Start date: September 2013
Phase: N/A
Study type: Interventional

The main purpose of this study is to examine changes in patient-reported symptoms during the first two cycles of neoadjuvant or adjuvant chemotherapy for non-small cell lung cancer (NSCLC), colorectal cancer (CRC) and breast cancer, among patients who receive standard care plus a proactive nursing intervention relative to patients who receive standard care alone. Interventions to improve symptom management and prevent urgent care needs in both the clinic and hospital for patients receiving chemotherapy with curative intent are needed to enhance the quality of cancer care.

NCT ID: NCT01943500 Completed - Breast Cancer Clinical Trials

Collection of Blood Specimens for Circulating Tumor Cell Analysis

Start date: September 30, 2013
Phase: N/A
Study type: Observational

Objective: To test the sensitivity of a proprietary novel filtration device designed to capture and concentrate circulating tumor cells (CTCs).

NCT ID: NCT01941953 Completed - Clinical trials for Metastatic Colorectal Cancer

Metformin and 5-fluorouracil for Refractory Colorectal Cancer.

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

This is a phase II trial to evaluate efficacy and safety of Metformin and Fluorouracil in patients with metastatic colorectal cancer (CRC) who have progressed after Oxaliplatin and Irinotecan based chemotherapy.

NCT ID: NCT01938300 Completed - Colorectal Cancer Clinical Trials

Magnesium and Rotational Thromboelastometry (ROTEM) in Colorectal Cancer Surgery

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

Magnesium sulphate is given to the patients during the colorectal cancer surgery under the hypothesis that it would attenuate the postoperative hypercoagulability. The investigators intend to characterize the changes of coagulation in colorectal cancer patients by using the point-of-care device after the infusion of magnesium sulphate.

NCT ID: NCT01932489 Completed - Metastatic Melanoma Clinical Trials

The Jules Bordet Institute Molecular Profiling Program Feasibility Trial

PRECISION-F
Start date: December 2013
Phase: N/A
Study type: Interventional

Prior to the use of genomic tests for patient inclusion in clinical trials, it is essential for the Jules Bordet Institute (JBI) to pilot the logistical and technical aspects by examining the feasibility and turnaround time of performing and obtaining data from a few key molecular assays. Patients with metastatic colorectal cancer, non-small cell lung cancer or melanoma will be enrolled. Biopsie from metastatic lesions will be performed. A targeted cancer gene screen assay will be performed using DNA sequencing. Results will be discussed during a molecular screening tumor board.