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Early Gastric Cancer clinical trials

View clinical trials related to Early Gastric Cancer.

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NCT ID: NCT02216110 Completed - Clinical trials for Early Gastric Cancer

Endoscopic Submucosal Dissection Versus Gastrectomy

Start date: May 2003
Phase: N/A
Study type: Observational

Gastrectomy is curative treatment for early gastric cancer (EGC). Recently, endoscopic submucosal dissection (ESD) has been accepted as standard treatment in selected patients with negligible risk of lymph node metastasis. However, there are limited data regarding the long-term outcomes of ESD in comparison with surgery. This protocol aims to compare overall survival rate, tumor recurrence, development of metachronous cancers after ESD and surgery.

NCT ID: NCT02189226 Completed - Clinical trials for Early Gastric Cancer

Usefulness of Probe-based Confocal Laser Endo-microscopy in Delineation of Margin of Early Gastric Cancer for Endoscopic Submucosal Dissection

Start date: November 2013
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the usefulness of pCLE (probe-based confocal laser endomicroscopy) compared with conventional chromoendoscopy (CE) for delineating the margin of early gastric cancer (EGC) with endoscopic submucosal dissection (ESD).

NCT ID: NCT02090062 Not yet recruiting - Clinical trials for Early Gastric Cancer

Difference in H. Pylori Infection Rate of EGC Patients Before and After Endoscopic Resection

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

Parts of patients are diagnosed as H. pylori -negative before ER, whereas the specimens become H. pylori-positive after ER, which may have a role in the recurrence of EGC. Our study aims to determine the difference in H. pylori infection rate of EGC patients before and after ER , and discuss the causes leading to the difference, which can provide references for improving the diagnostic accuracy of H. pylori infection and reducing EGC's recurrence rate.

NCT ID: NCT01938326 Completed - Clinical trials for Early Gastric Cancer

Pure Single Incision Laparoscopic Distal Gastrectomy (SIDG) Versus Totally Laparoscopic Distal Gastrectomy (TLDG)

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

1. Compare the immune response and postoperative complications between pure SIDG (single-incision laparoscopic distal gastrectomy) and TLDG (totally laparoscopic distal gastrectomy) for early gastric cancer (EGC) 2. Validate the safety, usefulness, minimal invasiveness and feasibility of SIDG (EGC)

NCT ID: NCT01921283 Completed - Clinical trials for Early Gastric Cancer

Monitored Anesthesia Care With Propofol Plus Remifentanil During Endoscopic Submucosal Dissection: Evaluation of Bispectral Index Monitoring

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

There are clinical usefulness issues associated with bispectral index (BIS) for sedation of endoscopic submucosal dissection (ESD). However, the clinical usefulness of BIS for deep sedation is incompletely described. The purpose of this study is to show that BIS-guided sedation is safe and useful clinically and may provide stable sedation status to physicians and patients.

NCT ID: NCT01832246 Not yet recruiting - Clinical trials for Early Gastric Cancer

Endoscopic Ultrasonographic Staging and Conventional Endoscopic Staging for Depth of Invasion for Early Gastric Cancer

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

The accurate prediction of depth of tumor invasion in early gastric cancer is essential for the proper selection of candidates for endoscopic resection. Conventional endoscopy and endoscopic ultrasonography have been useful diagnostic method for depth of invasion in early gastric cancer. However, there has been no prospective comparative study on the accuracy between the 2 methods. Therefore, the investigators prospectively compare the accuracy between the 2 methods regarding prediction of depth of invasion.

NCT ID: NCT01806753 Completed - Clinical trials for Early Gastric Cancer

Performance of Endoscopic Submucosal Dissection According to the Sedation Method

Start date: March 2013
Phase: N/A
Study type: Interventional

Although proper sedation is mandatory for endoscopic procedures such as endoscopic submucosal dissection, the effects of sedation on ESD performance and complications have not been fully evaluated. In the investigators previous retrospective study, en bloc resection and complete resection rates, and procedure time could be improved by sedation with continuous propofol infusion with opioid administration by anesthesiologists. However, there are several limitations to the study including retrospective design. The investigators aimed to evaluate the relationship among sedation methods, satisfaction of endoscopists or patients, clinical outcomes, and complications after endoscopic submucosal dissection for gastric neoplasia.

NCT ID: NCT01804998 Completed - Clinical trials for Early Gastric Cancer

Multicenter Phase III Trial of Laparoscopic Sentinel Node Biopsy

Start date: March 27, 2013
Phase: N/A
Study type: Interventional

Laparoscopic sentinel lymph node biopsy and stomach preserving surgery in early gastric cancer is less invasive method which can increase quality of life. For last two years, multicenter quality control study (Phase II) has been performed in Korea and tolerable results were observed. Based on these results, multicenter phase III trial is required to validate the clinical role of laparoscopic sentinel lymph node biopsy.

NCT ID: NCT01774266 Recruiting - Clinical trials for Early Gastric Cancer

Detection of Methylated Reprimo in Plasma for Asymptomatic Gastric Cancer

DEMRAC
Start date: September 2012
Phase: N/A
Study type: Observational

In this proposal the investigators aim to develop a commercial kit to be used in primary screening and non-invasive triage for early detection of gastric cancer. This kit will be cost-effective and more accessible to the general population. In addition, the investigators would like to expand our current patent already submitted to INAPI (National Institute for Intellectual Property) and propose royalties to biomedical diagnostic companies for the use of our product at international level.

NCT ID: NCT01688687 Completed - Clinical trials for Early Gastric Cancer

Conventional Biopsies vs pCLE for Diagnosis of Superficial Gastric Neoplasia

pCLE
Start date: February 2012
Phase: N/A
Study type: Observational

Confocal endomicroscopy (CLE) allows real-time in-vivo high-resolution and high-magnification imaging of the gastrointestinal epithelium, which is comparable to histopathology. Previous studies have investigated the accuracy of pCLE for diagnosis and differentiated of colorectal polyps, Barrett's esophagus and pancreaticobiliary strictures. However, to date there are limited data exploring the application of pCLE to gastric lesions, and this is the first study comparing the diagnosis of conventional forceps biopsy with that of pCLE using the final specimens obtained from endoscopic resection as a reference standard. The aims of this study were (1) the accuracy of pCLE compared to conventional forceps biopsy using histopathology results following endoscopic resection as a reference, and (2) comparison of "real time" in-vivo pCLE diagnosis with that of blinded "off-line" pCLE diagnosis, and off-line interobserver agreement.