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Gastrointestinal Neoplasms clinical trials

View clinical trials related to Gastrointestinal Neoplasms.

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NCT ID: NCT02487017 Recruiting - Clinical trials for Hepatocellular Carcinoma

DC-CIK Combined With TACE in the Treatment of Hepatocellular Carcinoma

Start date: May 2015
Phase: Phase 2
Study type: Interventional

Evaluation of DC-CIK cells combined TACE treatment for HCC

NCT ID: NCT02450656 Recruiting - Clinical trials for Carcinoma, Non-Small-Cell Lung

Afatinib and Selumetinib in Advanced KRAS Mutant and PIK3CA Wildtype Non-small Cell Lung Cancer

M14AFS
Start date: June 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This is a multi-center open-label proof-of-concept study consisting of two parts: PART A - a phase I dose-finding study (3 + 3 classical design) evaluating the RP2D of afatinib in combination with selumetinib in KRASm NSCLC; and PART B - a randomized phase II study investigating the progression free survival and safety of selumetinib/afatinib combination therapy compared to standard of care chemotherapy in KRASm NSCLC.

NCT ID: NCT02356406 Recruiting - Clinical trials for Digestive System Neoplasms

Celiac Plexus Radiosurgery for Pain Management

Start date: January 2014
Phase: Phase 2
Study type: Interventional

This prospective study evaluates celiac plexus radiosurgery for pain control in patients with upper abdominal malignancies.

NCT ID: NCT02349958 Recruiting - Ovarian Cancer Clinical Trials

Clinical Trial of Intraperitoneal Hyperthermic Chemotherapy

HIPEC/IPHC
Start date: September 2006
Phase: Phase 2
Study type: Interventional

To determine treatment response to surgical debulking and intra-operative Intraperitoneal Hyperthermic Chemotherapy (IPHC) in patients with the following malignancies: Gynecologic cancers (ovarian, primary peritoneal or fallopian tube, and uterine/cervical cancers). Mesotheliomas. GI cancers (Gallbladder, liver, small intestine, pancreas, stomach, colon, appendix). To monitor the toxicities and complications of this treatment regimen. To measure treatment related QOL changes after IPHC.

NCT ID: NCT02233205 Recruiting - Clinical trials for Gastrointestinal Neoplasms

Safety Study of Combining Ultrasound Microbubbles and Chemotherapy to Treat Malignant Neoplasms of Digestive System

Start date: October 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Ultrasonic sonoporation can increase the release of chemotherapeutics, thus increasing the therapeutic effects. The main purpose is to identify the safety of combining ultrasonic microbubbles and chemotherapeutics to treat malignant neoplasms of hepatic metastases from alimentary system and pancreatic carcinoma.

NCT ID: NCT02231476 Recruiting - Clinical trials for Gastrointestinal Cancer

Efficacy of Radiotherapy in Combination With Zoledronic Acid on Pain Relief in Bone Metastasis Patients

Start date: November 2014
Phase: Phase 2
Study type: Interventional

Bone metastasis causes bone destruction and skeletal related events (SRE) including compression fracture, hypercalcemia, and spinal cord compression. Therefore, palliative treatments for pain control and local control have become important and multidisciplinary multimodality approach is needed for treatment of bone metastasis. The efficacy of radiotherapy (RT) for bone metastasis is well known. And the results that bisphosphonate decreases SRE in patients with solid tumor and multiple myeloma reported. In previous retrospective reports, the combination of local RT and systemic bisphosphonate was more effective than RT alone. Therefore, the investigators designed a phase II study to evaluate the efficacy of RT in combination with zoledronic acid on pain relief and the safety of RT in bone metastasis patients with gastrointestinal tumors.

NCT ID: NCT02226224 Recruiting - Clinical trials for Gastrointestinal Neoplasms

Endoscopic Ultrasound in Detailed T-staging of Upper GI Malignancies in Vitro

Start date: June 2014
Phase: N/A
Study type: Observational

In our era of personalized treatment, both the prognosis and the choice of therapy for upper GI malignancies depend on the staging before any treatment. Most experts recommend EUS (Endoscopic Ultrasound) as the first line for T-staging but the diagnostic accuracy in clinical practice varies in different centers according to the published data. Neither the discrepancy between EUS and histological findings nor the variation between centers well explained. So the investigators designed this prospective study. In the present study, the investigators performed EUS on the resected specimen after surgery before fixation in formalin, evaluated the invasion of the GI wall, and marked the deepest location with sutures. And try to determine the exact accuracy of EUS staging , find the discrepancy between EUS and histologic findings.

NCT ID: NCT02208804 Recruiting - Clinical trials for Colorectal Neoplasms

Surefire Infusion System vs. Standard Microcatheter Use During Holmium-166 Radioembolization

SIM
Start date: November 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of the SIM trial is to investigate whether using the Surefire Infusion System during holmium-166 radioembolization increases the posttreatment tumor to non-tumor activity concentration ratio, compared with using a standard end-hole microcatheter.

NCT ID: NCT02196935 Recruiting - Pancreatitis Clinical Trials

Los Angeles Prospective GI Biliary and EUS Series

Start date: September 2010
Phase:
Study type: Observational

Endoscopic retrograde cholangiopancreatography and endoscopic ultrasound are increasingly being used to manage complex disease of the bile duct, pancreas and cancer. Gastroenterology patients at the Los Angeles County Hospital presents a unique and diverse patient population. Our aim is to study the biochemical, radiographic, and clinical predictors of bile duct stones. Exploratory aims include the study of the management of cholangitis, bile leaks, GI cancer diagnosis and management, and the management of pancreaticobiliary problems in the underserved. All patients managed by EUS or ERCP at the LA County & USC University Hospitals will be enrolled in the databaseThe timing, clinical presentation, and objective details of patient presentation are recorded prospectively. Additionally the results of the subsequent ERCP and EUS procedures. Subsequent, clinical course and pathology will also be recorded.

NCT ID: NCT02169388 Recruiting - Colorectal Cancer Clinical Trials

Intestinal Microflora in Colorectal Cancer (CRC) After Chemotherapy

Start date: June 2014
Phase: Phase 1
Study type: Interventional

Probiotics modulate the gut microflora and immune status in CRC,which can reduce the side effects of chemotherapy such as diarrhea,infection,neutropenia etc.