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Locally Advanced Rectal Cancer clinical trials

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NCT ID: NCT03064646 Recruiting - Clinical trials for LOCALLY ADVANCED RECTAL CANCER

Organ Preservation in Locally Advanced Rectal Cancer

PRONAR
Start date: March 10, 2017
Phase: N/A
Study type: Interventional

PRONAR trial aims to assess if treatment with organ preservation in stage II and III rectal cancer after a complete or almost complete response to neoadjuvant treatment is feasible and safe in our environment. The main objective of this project is to implement the organ preservation strategy in the treatment of rectal cancer in our environment within a clinical study that allows the analysis of its results in terms of survival. The secondary objective is to assess local relapse, distant relapse and quality of life.

NCT ID: NCT03040180 Recruiting - Neoadjuvant Therapy Clinical Trials

Endoscopic Assisted Electrochemotherapy in Addition to Neoadjuvant Treatment of Locally Advanced Rectal Cancer

nECT
Start date: January 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of neoadjuvant electrochemotherapy on locally advanced rectal cancer (UICC II-III) in an intended curative clinical setting, using an endoscopic electroporation device (EndoVE).

NCT ID: NCT02964468 Recruiting - Clinical trials for Locally Advanced Rectal Cancer

Dose-escalation Trial of Preoperative Radiotherapy and Concurrent Chemotherapy in Locally Advanced Rectal Cancer

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

The aim of this study is to evaluate the increase of radiation dose administered in patients diagnosed with locally advanced rectal cancer in terms of ypRC with tolerable toxicity, using IMRT (concomitant boost technique).

NCT ID: NCT02605265 Recruiting - Clinical trials for Locally Advanced Rectal Cancer

Trial of Capecitabine With or Without Irinotecan Driven by UGT1A1

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

The study evaluate the addition of Irinotecan in neoadjuvant chemoradiation. Half of participants will receive capecitabine alone together with neoadjuvant CRT, followed by a cycle of XELOX, while the other will receive capecitabine and irinotecan during CRT, followed by a cycle of XELIRI. All participants will be scheduled to receive surgery 6-8 weeks after the completion of CRT, then 5 cycles of adjuvant chemotherapy of XELOX.

NCT ID: NCT01899118 Recruiting - Clinical trials for Locally Advanced Rectal Cancer

Nimotuzumab in Combination With Chemoradiation in Patients With Locally Advanced Rectal Cancer

Start date: April 2013
Phase: Phase 2
Study type: Interventional

Neoadjuvant (preoperative) concomitant chemoradiotherapy (CRT) is now considered as a standard treatment of locally advanced rectal adenocarcinomas, which correlates better local control and higher sphincter preservation rate. Nimotuzumab, a humanized monoclonal antibody against epidermal growth factor receptor (EGFR) has been reported to improve the therapeutic effect of radiotherapy in some cancers. This study is a clinical phase II trial designed to evaluate the efficacy of the combination of Nimotuzumab administered concurrently with neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer, and to further investigate its side-effect and toxicity.