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Rectal Cancer clinical trials

View clinical trials related to Rectal Cancer.

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NCT ID: NCT01865071 Recruiting - Rectal Cancer Clinical Trials

Early Closure of Temporary Loop Ileostomy After Rectal Resection for Cancer

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

Early Closure of Temporary Loop Ileostomy After Rectal Resection for cancer

NCT ID: NCT01863862 Recruiting - Rectal Cancer Clinical Trials

Organ Preservation in Elderly Patients With Rectal Cancer

Start date: August 2012
Phase: N/A
Study type: Interventional

In elderly patients postoperative mortality measured 3-6 months after total mesorectal excision is high. Thus, less toxic treatments may lead to a survival benefit for elderly patients even if a risk of local recurrence is slightly higher compared to the open surgery. The investigators addressed the question whether watch and wait policy is safe in clinical complete responders after (chemo)radiation for elderly patients with small or moderately advanced tumours.

NCT ID: NCT01863420 Unknown status - Gastric Cancer Clinical Trials

The Effect of Bone Marrow-sparing Intensity-Modulated Radiotherapy to GI Cancer

IMRT
Start date: November 2012
Phase: Phase 2
Study type: Observational [Patient Registry]

Concurrent chemotherapy with external beam radiotherapy is the standard treatment of bulky or locally advanced cervical cancer, gastric cancer and rectal cancer.Despite excellent therapeutic results, acute hematologic toxicity (HT) is common with this regimen. Previous studies have founded acute HT was significantly associated the volume of pelvic (PBM) and lumbosacral bone marrow (LSBM) receiving 10 and 20 Gy radiation (RT). Therefore, reducing the volume of BM receiving low-dose RT might prevent HT. More than one-half of the body's bone marrow (BM) is located in the PBM, LSBM and proximal, where is just in the low dose of RT in patients with gastric, rectal and cervical cancer. Previous study have demonstrated highly conformal IMRT treatment plans reduced the volume of PBM irradiated resulting in less HT. We have since assumed that even better BM sparing is possible when the BM is entered as a separate constraint in the planning process. However, it is well known that hematopoietically active (red) BM is poorly visualized with computed tomography (CT). Consequently, the entire contents of the medullary canals must be entered as BM. Yet, a considerable portion of the medullary canal is comprised of inactive (yellow) marrow, which is composed primarily of fat. Contouring the entire medullary canals on CT thus overestimates the volume of active BM, unnecessarily constraining the IMRT plan. An alternative approach is the incorporation of functional BM imaging into the treatment planning process. One economical and efficiency approach involves the use of T1-weighted magnetic resonance (MR) images. Therefore, we designed this study to test whether a separate constraint of active BM identified by MR could reduce acute HT in course of concurrent chemoradiotherapy for patients with gastric and rectal cancer.

NCT ID: NCT01861678 Active, not recruiting - Rectal Cancer Clinical Trials

Randomized Controlled Trial to Evaluate High Tie Versus Low Tie of the Inferior Mesenteric Artery in Anterior Resection

Start date: July 2006
Phase: Phase 3
Study type: Interventional

The tying at a radix of the inferior mesenteric artery (IMA) is recognized as radical cure technique in a rectal cancer surgery in Japan. In one side, the preserving the left colic artery (LCA) that is the technique to maintain blood flow of proximal sigmoid colon is performed in practice. However, there is no evidence that shows effectiveness of this technique. We conducted a randomized trial that compared between high tie and low tie of the IMA in rectal anterior resection to define an appropriate portion of IMA tying.

NCT ID: NCT01836926 Completed - Rectal Cancer Clinical Trials

TaTME Versus Open Intersphincteric Resection After Neoadjuvant Concurrent Chemoradiotherapy.

TaTME
Start date: April 2013
Phase: N/A
Study type: Interventional

The two surgical options for lower 1/3 rectal cancer is APR and sphincter sparing procedures. Intersphincteric resection is procedure to treat very low rectal cancer within 2 cm from the dentate line to avoid permanent colostomy,improves the quality of life with better genitourinary function. Neoadjuvant chemo-radiotherapy is routine for T3 cases.

NCT ID: NCT01835925 Completed - Rectal Cancer Clinical Trials

Rectal Cancer Consortium

Start date: July 2013
Phase: N/A
Study type: Observational

The purpose of this study is to study which genes are abnormal in rectal cancer and see if this predicts how well chemotherapy and radiation will reduce the size of cancer and whether cancer recurs after surgery.

NCT ID: NCT01830582 Completed - Rectal Cancer Clinical Trials

Advanced MR Imaging for Early Biologic Tumor Changes to Neoadjuvant Chemoradiation Treatment for Rectal Cancer

Start date: April 9, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to see whether three new types of MRI techniques used during magnetic resonance imaging (MRI) of the pelvis to look at rectal cancer can help doctors to tell if the tumor is getting better in response to the radiation and/or chemotherapy treatments.

NCT ID: NCT01818973 Recruiting - Rectal Cancer Clinical Trials

Preoporative Bevacizumab, Radiation Therapy, and XELOX Chemotherapy for Locally Advanced Nonmetastatic Rectal Cancer

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

We presumed that the addition of a monoclonal antibody Bevacizumab into radiation therapy and combination chemotherapy could results in improved pathologic tumor regression grade (TRG) in locally advanced nonmetastatic rectal cancer.

NCT ID: NCT01814969 Recruiting - Rectal Cancer Clinical Trials

Preoperative Hyperfractionated Radiotherapy or Radiochemotherapy in Locally Advanced Rectal Cancer.

Start date: March 2014
Phase: Phase 3
Study type: Interventional

Clinical objective of the study is to compare the rates of pathologic response, acute toxicity and sphincter preservation with two schedules of preoperative regiment in patients with locally advanced rectal cancer.

NCT ID: NCT01801059 Completed - Rectal Cancer Clinical Trials

Patient Activation Intervention in Improving Screening Rates for Colorectal Cancer

Start date: September 2007
Phase: N/A
Study type: Interventional

This randomized clinical trial focused on activating the patient to ask their health care provider for a colorectal cancer screening test to improve screening rates for colorectal cancer. The patient activation intervention may increase information seeking, number of screening tests ordered and number of completed screening tests for colorectal cancer.