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Stomach Neoplasms clinical trials

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NCT ID: NCT02450032 Completed - Gastric Cancer Clinical Trials

Study to Determine the Antibody Response to 500µg G17DT in Treatment of Patients With Gastric Cancer

GC5
Start date: February 2000
Phase: Phase 2
Study type: Interventional

This study was designed to investigate the antibody response generated by a 500µg dose of G17DT in patients with gastric cancer.

NCT ID: NCT02444897 Completed - Gastric Cancer Clinical Trials

The Comparison Between Epidural and Intravenous Patient-controlled Analgesia for Laparoscopic Gastrectomy

Start date: September 2013
Phase: Phase 3
Study type: Interventional

This study was designed to assess the effectiveness of epidural patient-controlled analgesia compared to intravenous patient-controlled analgesia in patients undergoing laparoscopic gastrectomy. The investigators hypothesized that epidural PCA would be more effective in pain control than IV PCA even for laparoscopic gastrectomy.

NCT ID: NCT02442362 Completed - Gastric Cancer Clinical Trials

TOF Versus SOX in Metastatic Gastric Cancer

Start date: January 2012
Phase: Phase 2/Phase 3
Study type: Interventional

This study was designed to compare the efficacy and safety of aclitaxel/oxaliplatin/fluorouracil (TOF) regimen and S-1/oxaliplatin (SOX) regimen for metastatic gastric cancer (GC) patients.

NCT ID: NCT02435108 Completed - Clinical trials for c-MET Positive Gastric Cancer

A Pilot Study of Crizotinib in Patients With c-MET Positive Gastric Adenocarcinoma as a Third-line Chemotherapy

Start date: May 15, 2014
Phase: Phase 2
Study type: Interventional

This is a pilot study of crizotinib in patients with c-MET positive gastric adenocarcinoma.

NCT ID: NCT02430636 Completed - Stomach Neoplasms Clinical Trials

Irreversible Electroporation(IRE) For Unresectable Stomach Neoplasms

IRE
Start date: January 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of irreversible electroporation (IRE) for unresectable Stomach Neoplasms.

NCT ID: NCT02425930 Completed - Gastric Cancer Clinical Trials

The Predictive Value of Complement C3 in Patients With Advanced Gastric Cancer

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

This study is designed to investigate whether complement C3 depletion is associated with poor short-term outcomes in postoperative patients with gastric cancer.

NCT ID: NCT02415023 Completed - Gastric Cancer Clinical Trials

A Phase Ib/2 Clinical Study of Fruquintinib Combined With Paclitaxel in the Treatment of Advanced Gastric Cancer

Start date: November 9, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

An open-label, dose escalation and maximum tolerated dose (MTD) and/or recommended phase II dose (RPTD) study of fruquintinib combined with paclitaxel in patients with advanced gastric cancer who did not respond to first-line standard chemotherapy.

NCT ID: NCT02406170 Completed - Neoplasm Metastasis Clinical Trials

Regorafenib in Combination With Paclitaxel in Advanced Oesophagogastric Carcinoma

REPEAT
Start date: April 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Patients with advanced oesophagogastric cancer (OCG) have a very poor prognosis. After progression on first line therapy, second line chemotherapy with paclitaxel and a VEGF-R2 targeting antibody has a proven benefit on survival. However, no data are available on the combination of paclitaxel with kinase inhibitors in advanced OGC. Here the investigators propose a Phase 1b study to assess the tolerability of regorafenib (an oral multi kinase inhibitor) in combination with paclitaxel and to assess the uptake of paclitaxel in OCG metastasis.

NCT ID: NCT02395640 Completed - Gastric Cancer Clinical Trials

The Comparison of XELOX and EOX in the First-line Treatment of Advanced Gastric Cancer

Start date: March 2015
Phase: Phase 3
Study type: Interventional

This study is designed to compare the efficacy and safety of XELOX regimen with EOX regimen in the first-line treatment of advanced gastric cancer patients.

NCT ID: NCT02385630 Completed - Weight Loss Clinical Trials

Longitudinal Assessment of Gut Hormone Secretion Following Upper Gastrointestinal Surgery for Cancer

Start date: March 2015
Phase: N/A
Study type: Interventional

Surgery is the cornerstone of treatment for patients with oesophageal or gastric cancer, but while surgical removal of the tumour (oesophagectomy or gastrectomy) may offer the best chance of cure, these are major operations associated with specific long term complications. Weight loss and poor nutrition are relatively common problems among patients who attain long-term cancer remission and cure after surgery. The mechanisms underlying these problems are not well understood and therefore treatment options are limited. The investigators research has demonstrated increased levels of chemical messengers (gut hormones) released from the gastrointestinal tract after meals in patients who have previously undergone upper gastrointestinal surgery. These chemical messengers play a role in signalling the feeling of fullness during and after a meal (satiety). Understanding the mechanisms involved in increased gut hormone secretion after these operations may allow us to use certain medications to block gut hormone release and hence reduce satiety allowing patients to eat more, regain weight and prevent nutritional complications after surgery. Exaggerated post-prandial satiety gut hormone responses following oesophagectomy have, however, only been established cross-sectionally and therefore the time course for development of increased gut hormone secretion is unknown. Data collected from this study will provide important information about optimal timing of therapeutic intervention in this patient group, while offering mechanistic insights with regard to the pathophysiologic process underlying post-operative early satiety.