Clinical Trials Logo

Colon Cancer clinical trials

View clinical trials related to Colon Cancer.

Filter by:

NCT ID: NCT03826446 Completed - Colon Cancer Clinical Trials

Laparoscopic Versus Open Complete Mesocolic Excision With Central Vascular Ligation in Right Colon Cancer

Start date: January 13, 2016
Phase: N/A
Study type: Interventional

Right sided hemicolectomy is the standard type of operation for cancers in the caecum, the ascending colon.The aim of this study was to compare between laparoscopic and open complete mesocolic excision with central vascular ligation in right colon cancer.

NCT ID: NCT03801915 Completed - Pancreatic Cancer Clinical Trials

Perioperative MVT-5873, a Fully Human Monoclonal Antibody Against a CA 19-9 Epitope, for Operable CA 19-9 Producing Pancreatic Cancers, Cholangiocarcinomas, and Metastatic Colorectal Cancers

Start date: November 13, 2019
Phase: Phase 2
Study type: Interventional

Background: Gastrointestinal tumors have a molecule called carbohydrate antigen 19-9 (CA19-9) in the tumors and blood. The agent MVT-5873 was designed to block this molecule. Researchers want to test how safe it is to give this agent to people before and after surgery to remove a tumor. They want to learn the highest dose tolerated. They want to see if getting the agent at surgery helps slow down the disease. Objective: To test the safety of giving MVT-5873 at surgery to remove cancer and see if it slows the progression of the disease. Eligibility: Adults at least 18 years old with certain cancers and certain blood CA19-9 levels Design: Participants will be screened with: - Medical history - Physical exam - Blood and heart tests - Scans - Review of normal activities - Review of tumor sample - Pregnancy test A few days before surgery, participants will get a dose of the study agent. They will get it through a small plastic tube in a vein over about 2 hours. Participants will sign a separate consent and have the surgery. A sample of the tumor and normal liver will be removed for research. For 1-2 weeks after surgery, participants will recover in intensive care then regular care at the hospital. They will be monitored and treated throughout the stay. After leaving the hospital, participants will get the study agent every week for 1 month. Then they will get it every other week for 2 months. They will repeat screening tests at study visits and at a follow-up visit. That will be about 5 weeks after the last dose.

NCT ID: NCT03794193 Active, not recruiting - Colon Cancer Clinical Trials

The Effect of Unfavorable Histological Features on the Oncological Outcomes of Colon Cancer

Start date: January 1, 2016
Phase:
Study type: Observational

To explore the effect of unfavorable histological features on the clinical outcomes of patients receiving radical resection of colon cancer.

NCT ID: NCT03781778 Terminated - Rectal Cancer Clinical Trials

Pilot Trial of Resistant Starch in Stage I-III Colorectal Cancer Survivors

Start date: May 7, 2019
Phase: Phase 2
Study type: Interventional

This phase II, randomized pilot trial studies the effect of the consumption of foods made with resistant starch compared to foods made with corn starch on biomarkers that may be related to colorectal cancer progression in stage I-III colorectal cancer survivors. Foods made with resistant starch may beneficially influence markers of inflammation, insulin resistance, and the composition of gut bacteria in colorectal cancer survivors.

NCT ID: NCT03779009 Recruiting - Colon Cancer Clinical Trials

Minimally INvasive Colon Cancer Surgery Through IMmunomics and Optical Mapping of the Sentinel Lymph Node.

MINIMAL
Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The project investigates the feasibility of laparoscopic fluorescent imaging for the intraoperative detection of the sentinel lymph node (SLN) in colon cancer patients. In addition, the topology of immunological and microenvironmental changes in normal and invaded lymph nodes (LN's) will be correlated to the LN location (anatomical mapping).

NCT ID: NCT03774680 Recruiting - Colon Cancer Clinical Trials

Targeted Polymeric Nanoparticles Loaded With Cetuximab and Decorated With Somatostatin Analogue to Colon Cancer

Start date: February 1, 2020
Phase: Phase 1
Study type: Interventional

Due to the great toxicity of chemotherapeutic drugs to both the healthy and cancerous area, the efficient targeting could be of great benefit for a patient with advanced or metastatic tumors. Colorectal cells carry somatostatin receptors which make them a promising target for antitumor therapy since this would reduce side effects and increase drug delivery efficacy to the target site.

NCT ID: NCT03750461 Completed - Rectal Cancer Clinical Trials

Stoma Closure and Reinforcement Trial

SCAR
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Hernia formation at sites of ostomy closure is a common complication. The investigator believes that using evidence based hernia repair techniques as a preventive measure during closure of ostomies will reduce the incidence of hernia formation. In this trial, the investigator will pilot a novel technique of large pore monofilament polypropylene mesh reinforcement of the abdominal wall defects that remain after closure of an ileostomy to evaluate for safety and begin to evaluate the effectiveness compared to standard techniques.

NCT ID: NCT03745326 Recruiting - Pancreatic Cancer Clinical Trials

Administering Peripheral Blood Lymphocytes Transduced With a Murine T-Cell Receptor Recognizing the G12D Variant of Mutated RAS in HLA-A*11:01 Patients

Start date: May 16, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Background: A new cancer therapy takes white blood cells from a person, grows them in a lab, genetically changes them, then gives them back to the person. Researchers think this may help attack tumors in people with certain cancers. It is called gene transfer using anti-KRAS G12D mTCR cells. Objective: To see if anti-KRAS G12D mTCR cells are safe and cause tumors to shrink. Eligibility: Adults ages 18-72 who have cancer with a molecule on the tumors that can be recognized by the study cells Design: Participants will be screened with medical history, physical exam, scans, photography, and heart, lung, and lab tests. An intravenous (IV) catheter will be placed in a large vein in the chest. Participants will have leukapheresis. Blood will be removed through a needle in an arm. A machine will divide the blood and collect white blood cells. The rest of the blood will be returned to the participant through a needle in the other arm. A few weeks later, participants will have a hospital stay. They will: - Get 2 chemotherapy medicines by IV over 5 days. - Get the changed cells through the catheter. Get up to 9 doses of a medicine to help the cells. They may get a shot to stimulate blood cells. - Recover in the hospital for up to 3 weeks. They will provide blood samples. Participants will take an antibiotic for at least 6 months. Participants will have several follow-up visits over 2 years. They will repeat most of the screening tests and may have leukapheresis. Participants blood will be collected for several years.

NCT ID: NCT03725176 Completed - Colon Cancer Clinical Trials

An Open Label Trial Examining Web Based Colonoscopy Preparation Instruction

Start date: April 6, 2016
Phase:
Study type: Observational

Current pre-colonoscopy instructions are given to patients in the form of a written or printed instruction set. We have developed a web-based instruction system which aims to provide a more effective instructional experience for the patient in hopes in increase their adherence to pre-colonoscopy guidelines. After trialing this approach, we are ready to implement this medium of instruction for all patients receiving colonoscopies.

NCT ID: NCT03719573 Completed - Colorectal Cancer Clinical Trials

Geriatric Assessment and Intervention in Older Patients Undergoing Surgery for Colorectal Cancer

GEPOC
Start date: February 21, 2019
Phase: N/A
Study type: Interventional

The GEPOC study investigates the effect of comprehensive geriatric assessment and intervention for frail older patients (65 years or older) undergoing elective surgery for colorectal cancer. the geriatric intervention will be pre- and postoperative. included in the intervention is an exercise intervention. The main aim of the study us to see if the functional decline in this group can be reduced.