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Rectal Neoplasms clinical trials

View clinical trials related to Rectal Neoplasms.

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NCT ID: NCT03749083 Withdrawn - Clinical trials for Gastrointestinal Malignancies

A Study of the Role of Circulating Tumor DNA in Predicting the Likelihood of Organ Preservation After Clinical Complete Response to Neoadjuvant Therapy for Rectal Cancer

Start date: December 31, 2019
Phase:
Study type: Observational

In this research study, the investigators are looking to see if the circulating tumor DNA (genetic material), also known as ctDNA, in the blood will help them predict whether the participant's cancer will come back.

NCT ID: NCT03741166 Completed - Colo-rectal Cancer Clinical Trials

Blood Collection Sub-Study for CRC Screening in Individuals 45-49 at Average Risk for CRC.

Start date: November 8, 2018
Phase:
Study type: Observational

The primary objective of this sub-study, 2018-10B, is to collect blood specimens to assess new biomarkers for the detection of Colorectal Cancer (CRC).

NCT ID: NCT03735407 Completed - Colo-rectal Cancer Clinical Trials

Safety,Usability and Compliance of Using C-Scan System for Providing Information on Colonic Polypoid Lesions and Masses

C-Scan
Start date: February 1, 2019
Phase: N/A
Study type: Interventional

Protocol Title: Evaluation of safety, usability and subject compliance while using Check- Cap's C-Scan System for providing structural information on colonic polypoid lesions and masses Study Design: Prospective, Multi-center, Single-arm, safety study Purpose: To demonstrate the safety of the Check-Cap C-Scan System Study Centers: Up to two (2) centers located in the United States Number of Participants: 45 healthy subjects Investigational Device: Check-Cap's C-Scan System comprises C-Scan Capsule, C-Scan Track and C-Scan View. Primary Objective: To evaluate the safety of the Check-Cap C-Scan System Secondary Objectives: a. To evaluate subject's compliance b. To evaluate subject's satisfaction c. To collect data to improve the product's algorithm

NCT ID: NCT03731754 Not yet recruiting - Rectal Cancer Clinical Trials

"Cross" Closure for Reconstructing the Perineal Wound of Abdominoperineal Resection

CCRPWAR
Start date: November 20, 2018
Phase: N/A
Study type: Interventional

How to reduce the complications of perineal wound after abdominoperineal resection (APR) has always been a hot topic in the medical field.To reduce the complications of perineal wound and the primary healing of perineal wound must meet the two principles of "unobstructed drainage" and " reduced tension closure".This concept is similar to the concepts of closure of enterostomy in rectal cancer patients. It was reported that use of cross-stitch closure can significantly reduce complications of closure of enterostomy. So the investigator ever used the "cross" closure to reconstruct the perineal wound of APR, which was really decrease the complications of perineal wound. However, more clinical trails was needed to confirm the conclusion.

NCT ID: NCT03731130 Recruiting - Quality of Life Clinical Trials

Prospective Observational Trial to Evaluate Quality of Life After Neoadjuvant Radiation or Chemoradiation Followed by Surgery in Patients With Rectal Cancer

NEOCARE
Start date: October 5, 2018
Phase:
Study type: Observational

Observational study to evaluate longitudinal quality of life according to standardized EORTC questionaires as well as functional Outcome, oncological outcome and toxicity in patients treated with neoadjuvant short term radiation or long-term chemoradiation followed by surgery

NCT ID: NCT03729687 Active, not recruiting - Rectal Cancer Clinical Trials

Short Course Radiation Therapy Followed by Pre-operative Chemotherapy and Surgery in High-risk Rectal Cancer

LARCT-US
Start date: July 4, 2016
Phase: Phase 2
Study type: Interventional

Patients with a primary rectal cancer without detectable distant metastasis who after locoregional therapy only, meaning preoperative radio(chemo)therapy plus surgery have at least a 40% risk of not having a CRM negative resection or a recurrence, local or distant, within three years will be treated with the short course 5 x 5 Gy radiation scheme followed by four cycles of combination chemotherapy (capecitabine and oxaliplatin) and TME surgery

NCT ID: NCT03724591 Not yet recruiting - Rectal Cancer Clinical Trials

Total Mesorectum Excision With Left Colic Artery Preservation for the Treatment of Rectal Cancer

Start date: January 2019
Phase: N/A
Study type: Interventional

A randomized controlled clinical trial to compare the short and long term outcomes of left colic artery preservation for the treatment of Rectal Cancer

NCT ID: NCT03718351 Recruiting - Early Rectal Cancer Clinical Trials

Endoscopic Submucosal Dissection Versus Transanal Endoscopic Microsurgery For Early Rectal Neoplasms And Large Rectal Adenomas: Сomparison Of Treatment Efficacy And Safety.

Start date: September 24, 2018
Phase: N/A
Study type: Interventional

Transanal endoscopic microsurgery is the main treatment option for rectal tumors such as large adenoma, early cancer because of lower complications and mortality rates and shorter hospital stays rather than conventional surgery. Particularly, However, transanal endoscopic microsurgerymust be performed under either general or spinal anesthesia, and expensive surgical instruments are required. Colorectal endoscopic submucosal dissection is a novel endoscopic procedure that enables en bloc resection of benign colorectal lesions and early colorectal cancer. Endoscopic submucosal dissectioncan be performed under conscious sedation without anesthesia, and there are fewer hospital days than those for transanal endoscopic microsurgery. In the present study, we compared the treatment efficacy and safety between endoscopic submucosal dissectionand transanal endoscopic microsurgery for the treatment of early rectal neoplasms and large rectal adenomas.

NCT ID: NCT03714490 Recruiting - Rectal Neoplasms Clinical Trials

MRI Simulation-guided Boost in Short-course Preoperative Radiotherapy for Unresectable Rectal Cancer

SUNRISE
Start date: October 23, 2018
Phase: Phase 2
Study type: Interventional

Improvements in downstaging are required when using preoperative chemoradiation for unresectable rectal cancer. There is therefore a need to explore more effective schedules. The study arm will receive MRI simulation-guided boost in short-course preoperative radiotherapy followed by consolidation chemotherapy , which may enhance the shrinkage of tumor comparing with the concurrent chemoradiation.

NCT ID: NCT03702985 Recruiting - Clinical trials for Locally Advanced Rectal Cancer

Radiation-protection Effect of Amifostine in Locally Advanced Rectal Cancer

Start date: May 28, 2018
Phase: Phase 2
Study type: Interventional

The study evaluates the addition of Amifostine to capecitabine and irinotecan in neoadjuvant chemoradiation(CRT) in locally advanced rectal cancer. Half of participants will receive capecitabine and along with neoadjuvant radiotherapy, followed by a cycle of XELIRI, while the others will receive capecitabine and irinotecan added by amifostine 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 it will depends which regimens the patient would receive according to his or her pathological results.