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Colorectal Cancer clinical trials

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NCT ID: NCT02607072 Recruiting - Colorectal Cancer Clinical Trials

Aspirin for Prevention of Postsurgical Recurrence and Metastasis in Asian Colorectal Cancer Patients: a Multi-center Randomized Trial

APREMEC
Start date: October 2015
Phase: Phase 3
Study type: Interventional

Background: Evidence of high quality has suggested that acetylsalicylic acid (ASA)/aspirin effectively reduces colorectal adenoma incidence and recurrence rate, and several randomized controlled trials (RCTs) strongly indicate its potential to prevent colorectal cancer (CRC) initiation and progression and to decrease cancer-related mortality. However the role of aspirin supplied as an adjuvant agent in postsurgical CRC patients remains obscure, and a RCT is warranted for clarification. Aim: The APREMEC trial aims to investigate the potential preventative role of enteric-coated aspirin (100 mg and 200 mg daily) against postsurgical recurrence and metastasis among Asian CRC patients. Design: The investigators hypothesize that this large-scale multicenter randomized double-blind placebo-controlled trial will support that aspirin can reduce recurrence and metastasis and improve survival in postsurgical non-metastasized CRC patients. The primary endpoint of this trial is disease-free survival, and the secondary endpoints are 3-year and 5-year overall survival, the interactive effects of lifestyle including smoking and alcohol ingestion, and adverse event rate. Eligible postoperative patients with non-metastasized CRC will be randomized in this trial to 100 mg aspirin, 200 mg aspirin or placebo until recurrence/metastasis, severe adverse event, death, or end of study, after standard adjuvant therapy. Individuals with peptic ulcer, bleeding tendency, or previous or ongoing treatment with aspirin or other anticoagulants will be excluded from this trial. Stratification factors are gender, study center, cancer site, and tumor stage. After randomization, patients will be followed up with evaluations at a 3-month interval while taking study drug. Discussion: This study aims at investigation of aspirin's role as an adjuvant agent in prevention of postsurgical CRC recurrence and metastasis. If results turn out to be positive, Asian and global CRC patients will be greatly benefited, due to the fact that aspirin is inexpensive, easily-accessible, and simply-administered, with well know and managed adverse events.

NCT ID: NCT02591667 Recruiting - Colorectal Cancer Clinical Trials

Histopathological Response to FOLFOXIRI + Bevacizumab in Peritoneal Metastasis From Colorectal Cancer

CARCINOSIS
Start date: March 2016
Phase: Phase 2
Study type: Interventional

There is a paucity of data on the histopathological response of peritoneal tumor deposits from colorectal cancer to neoadjuvant chemotherapy. Particularly, no prospective assessment of chemotherapy-associated histopathological response within the peritoneum has been performed so far. Therefore, there is an urgent need to conduct a clinical trial aimed at prospectively assessing the histopathological response within the peritoneum in patients with peritoneal metastasis from colorectal cancer. Recently, Loupakis et al. reported that the triplet regimen of 5-fluorouracil, oxaliplatin and irinotecan (FOLFOXIRI) in combination with bevacizumab significantly improved median progression-free survival in metastatic colorectal cancer patients from 9.7 to 12.1 months as compared with fluorouracil, leucovorin, and irinotecan (FOLFIRI) + bevacizumab. In view of these data, it is likely that FOLFOXIRI + bevacizumab will also lead to a significant improvement of the histopathological response within the peritoneum of patients with peritoneal metastasis from colorectal cancer (pcCRC) as compared with previous standard chemotherapy. The investigators hypothesize that FOLFOXIRI + bevacizumab will induce a pCR or major response in peritoneal tumor deposits in >30% of patients (taking the response rate to FOLFOX- or FOLFIRI-based neoadjuvant chemotherapy from the published literature as a reference).

NCT ID: NCT02584244 Recruiting - Colorectal Cancer Clinical Trials

Feasibility of the LUM Imaging System for Detection of Gastrointestinal Cancers

Start date: August 4, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The overall goal of this feasibility study is to assess the initial safety and efficacy of LUM015 in ex vivo far-red imaging of colorectal, pancreatic, and esophageal cancers (adenocarcinoma) using the LUM Imaging System.

NCT ID: NCT02574013 Recruiting - Colorectal Cancer Clinical Trials

Randomized Controlled Trial for Retractor SPONGE Evaluation in Laparoscopic Colorectal Surgery

SPONGE
Start date: November 2015
Phase: N/A
Study type: Interventional

To achieve an adequate visual working field during laparoscopic colorectal surgery without disturbance of the small intestine, patients are positioned in Trendelenburg position. This position results in hemodynamic changes which may increase the risk of cardiopulmonary complications and prolonged hospital stay. Recently, an intraoperative retractor sponge was introduced as alternative for the Trendelenburg position during laparoscopic surgery.

NCT ID: NCT02571374 Recruiting - Colorectal Cancer Clinical Trials

Symbiotics to Prevent Postoperative Infection in Colorectal Cancer

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

This is a double blind randomized trial in which patients with colorectal cancer undergoing surgery will be selected to receive either a symbiotic formulation or placebo. The researchers will compare incidence of surgical site infection between the study groups.

NCT ID: NCT02562963 Recruiting - Colorectal Cancer Clinical Trials

Clinical Efficacy and Safety of NKT Cell Infusion in Patients With Advanced Solid Tumor

Start date: November 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Natural killer T (NKT) cells are a unique subset of lymphocytes that present a mixed T-NK phenotype. Our hypothesis is that Natural killer T cells may decrease the tumor burden and improve overall survival. The purpose of this study is to determine whether Natural killer T (NKT) cells are effective and safe in the treatment of patients with unresectable advanced solid tumor.

NCT ID: NCT02553031 Recruiting - Colorectal Cancer Clinical Trials

Application of MR-PET in Colorectal Cancer

Start date: July 2014
Phase: N/A
Study type: Observational

This study will explore the potential value in proper therapeutic decision and clinical outcome prediction by using integrated MR-PET system and advanced MR techniques in patients with colorectal cancer.

NCT ID: NCT02549456 Recruiting - Colorectal Cancer Clinical Trials

Natural Orifice Transluminal Endoscopic Surgery for Colorectal Cancer

NOTES
Start date: December 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess different hybrid natural orifice transluminal endoscopic surgery techniques in management of colorectal cancer as regard: feasibility of the technique, short term oncologic outcome and functional outcome.

NCT ID: NCT02545699 Recruiting - Colorectal Cancer Clinical Trials

Prospective Trial to Compare ADR of G-EYE™ Colonoscopy With Standard Colonoscopy

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the adenoma detection rate (ADR) of the G-EYE™ colonoscopy with that of standard colonoscopy.

NCT ID: NCT02531620 Recruiting - Colorectal Cancer Clinical Trials

Prehabilitation in Elective Colorectal Resection: A Pilot Study (Prehab)

Prehab
Start date: September 2015
Phase: N/A
Study type: Interventional

This is a pilot study designed to evaluate a programme of rehabilitation for patients undergoing elective colorectal resection surgery.