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Rectal Neoplasms clinical trials

View clinical trials related to Rectal Neoplasms.

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NCT ID: NCT03098108 Recruiting - Clinical trials for Previously Irradiated Recurrent Rectal Cancer

Concurrent Chemo-proton Radiotherapy With or Without Resection and Spacer Insertion for Loco-regional Recurrence of Previous Irradiated Rectal Cancer

RECCPT
Start date: February 9, 2017
Phase: N/A
Study type: Interventional

The investigators conduct this study to evaluate the efficacy and adverse effect of salvage concurrent chemo-proton therapy (CCPT) with or without surgical resection in previously irradiated recurrent rectal cancer.

NCT ID: NCT03074461 Recruiting - Rectal Cancer Clinical Trials

Transverse Coloplasty vs. Side-to-end Anastomosis Following Low Anterior Resection (LAR): CSAR Trial

CSAR
Start date: April 5, 2017
Phase: N/A
Study type: Interventional

CSAR Trial's aim is to determine whether the transverse coloplasty pouch or the side-to-end anastomosis as rectal reservoir reconstruction offers the best functional results.

NCT ID: NCT03071198 Recruiting - Rectum Cancer Clinical Trials

Clinical Effect of Neoadjuvant Hierarchical Treatment Based on Chemotherapy

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Clinical effect of neoadjuvant hierarchical treatment based on chemotherapy for T3-4N0-2M0 middle and lower rectal cancer

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: NCT03051464 Recruiting - Clinical trials for Stage II Rectal Cancer

No Surgery Trial / Two Dose-escalation Strategies

Morpheus
Start date: April 25, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

A randomized study of 145 patients. Patients with a clinical T2-3 N0 rectal cancer will be randomized to two arms (arm A: standard chemoradiation (45 Gy in 25 with concomitant 5-FU or Xeloda chemotherapy) and an external beam boost of 9 Gy compared to arm B: standard chemoradiation (45 Gy in 25 with concomitant 5-FU or Xeloda chemotherapy) and followed by a brachytherapy boost of 30 Gy in 3 fractions).

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: NCT03038256 Recruiting - Rectal Cancer Clinical Trials

Effect of Concurrent Capecitabine-based Long-term Radiotherapy Followed by XELOX Plus TME in Patients With High Risk Rectal Cancer: a Multi-centers, Randomized Controlled, Open-Label Trial

EXPLORE
Start date: January 31, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study was to evaluate the effect of concurrent capecitabine-based long-term radiotherapy followed by 4 cycles XELOX pre- a delayed TME compared with 6 cycles XELOX post- a Regular Timing TME in patients with high-risk rectal cancer defined by MRI.

NCT ID: NCT03022734 Recruiting - Clinical trials for Rectal Cancer, Metastatic

Short Course Radiotherapy, Unresectable Rectal Cancer, Liver Metastasis

Start date: September 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is the increase of resection rate of primary cancer in rectal after short course radiotherapy without interrupt chemotherapy schedule during the period of chemotherapy. Radiation therapy is followed by additional chemotherapy to prevent the progression of systemic metastasis, and to reduce the incidence of rectal carcinoma including metastasis.

NCT ID: NCT03013153 Recruiting - Rectal Cancer Clinical Trials

Low or High Ligation of the IMA With Apical Lymph Node Dissection in Rectal Cancer Laparoscopic Surgery

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

Laparoscopy colon surgery is accepted worldwide in the recent years. But there is still argument on the effect of laparoscopy rectal surgery. Laparoscopy has advantages on showing the inferior mesenteric artery (IMA), protection of autonomic nerve, low rectal anastomosis, and total mesorectum excision. However, debate on the level of IMA ligation and debonding of splenic flexure never ends. This study is going to give a clear and definite answer to how and why surgeons should deal with the IMA in laparoscopy rectal surgery,base on the 3D reconstruction of IMA and identification of IMA perfusion types.

NCT ID: NCT02979795 Recruiting - Rectal Cancer Clinical Trials

Translational Research in Identifying Molecular Mechanisms for Rectal Cancer Metastasis

Start date: November 2016
Phase: N/A
Study type: Observational [Patient Registry]

Rectal cancer, comprised of 30% of overall colorectal cancer cohort, is one of the leading cancers of Taiwan. In patients with advanced disease, the standard of care is concurrent chemoradiotherapy (CCRT) before surgery. After CCRT, the abscopal effect, a phenomenon that localized radiation not only destroys local tumor but also inhibits the growth of tumor at the remote site, has been observed. This effect is believed to be associated with tumor immune response. In addition, other immune checkpoint molecules, such as Programmed cell death-1(PD-1), Programmed cell death ligand-1 (PD-L1), and Cytotoxic T-Lymphocyte Associated Protein 4 (CTLA-4), have been reported associated with therapeutic outcome. However, after CCRT, more than 50% of patients were still either having persistent disease or developed distant metastasis. To improve therapeutic outcome of patients with rectal cancer, this project, thus, aims at exploring the evolution of factors that may affect the abscopal effect and immune checkpoint functions in tissues and in blood before and after CCRT.