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Esophagus Cancer clinical trials

View clinical trials related to Esophagus Cancer.

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NCT ID: NCT02530983 Recruiting - Esophageal Cancer Clinical Trials

Mayo Clinic Upper Digestive Disease Survey

UDD
Start date: August 2015
Phase:
Study type: Observational

The Mayo Clinic Conduit Report Card Questionnaires have been created in order to have a consistent evaluation tools for patients undergoing esophageal reconstruction or treatment or patients that are experiencing an upper digestive disease in order to standardize and validate outcome measures. Data will be used to establish the validation of the questionnaires/survey. Data will also lead to the establishment of "normal" or expected scores for patients undergoing each type of esophagectomy procedure and for upper digestive diseases. Data will contribute to creating treatment algorithms for symptom management for upper digestive diseases and for post-operative complications and symptoms as well as contribute to pre-operative education.

NCT ID: NCT02436018 Recruiting - Gastric Cancer Clinical Trials

WEI NASAL JET for The Sedation of Outpatient Upper Gastrointestinal Endoscopy

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

Low pulse oximetry is the most common adverse events during sedation for upper gastrointestinal endoscopy. The main reason is the glossoptosis after sedation. In present study a new designed nasopharyngeal airway embedded with jet ventilation catheter(WEI NASAL JET) will be utilized in order to reduce the hypoxia. At the same time the safety will be evaluated.

NCT ID: NCT02216149 Terminated - Colon Cancer Clinical Trials

Effects of S-1 and Capecitabine on Coronary Artery Blood Flow

FluoHeart
Start date: January 2015
Phase: Phase 2
Study type: Interventional

Fluoropyrimidine chemotherapy agents , such as 5-fluorouracil and capecitabine, are occasionally associated with cardiac toxicity. Clinical fluoropyrimidine cardiotoxicity is infrequent, but subclinical toxicity may be much more common. Cardiac toxicity may be less frequent with S-1 as compared with 5-fluorouracil and capecitabine, but head-to-head comparisons are lacking. The purpose of the study is to compare 2 measures of subclinical coronary artery microvascular dysfunction, the coronary flow reserve and the coronary flow response to a cold pressor test, in a patient population who are being treated for adenocarcinoma of the gastrointestinal tract with one of 2 oxaliplatin-containing regimens, either with oxaliplatin plus S-1 or with oxaliplatin plus capecitabine.

NCT ID: NCT02001623 Completed - Bladder Cancer Clinical Trials

Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors

Start date: November 30, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the trial is to establish the tolerability of HuMax-TF-ADC in a mixed population of patients with specified solid tumors.

NCT ID: NCT01979549 Recruiting - Gastric Cancer Clinical Trials

Adverse Events During Upper Gastrointestinal Endoscopy

AEDUGESSH
Start date: December 2013
Phase: N/A
Study type: Observational

The primary objective is to investigate the adverse events during upper gastrointestinal endoscopy with and without sedation in Chinese population

NCT ID: NCT01774851 Terminated - Stomach Cancer Clinical Trials

A Study of MM-111 and Paclitaxel With Trastuzumab in Patients HER2 Positive Carcinomas of the Distal Esophagus, Gastroesophageal (GE) Junction and Stomach

Start date: January 2013
Phase: Phase 2
Study type: Interventional

To determine whether the combination of MM-111 plus paclitaxel and trastuzumab is more effective than paclitaxel and trastuzumab alone

NCT ID: NCT01684904 Recruiting - Esophagus Cancer Clinical Trials

Proton Therapy for Esophageal Cancer

Start date: February 20, 2013
Phase: N/A
Study type: Interventional

The goal of this phase II study is to investigate the feasibility, toxicity and efficacy of a regimen incorporating a proven systemic regimen, carboplatin /paclitaxel, with conformal proton modality, followed by definitive surgery. In most combined-modality trials to date, chemotherapy regimens have included cisplatin, usually in conjunction with 5-fluorouracil. In designing the regimen, the investigators attempt to improve on the standard cisplatin/5-fluorouracil regimen in several ways. First, full-dose paclitaxel is added to the regimen. This agent has activity against advanced esophageal cancer and is also a potent radiosensitizer. Second, the substitution of carboplatin for cisplatin has resulted in reduced toxicity of various combination regimens similar to that used by CROSS trial and allows for easier administration in the outpatient setting.4 Third, for localized esophageal cancer, dose distribution patterns achievable with proton beam could potentially offer important clinical advantages relative to those achievable with x-rays (photons).19 Based on this, the investigators believe that this study should be conducted with the radiation modality that offers the best dosimetry achievable at our institution.

NCT ID: NCT01669356 Completed - Esophagus Cancer Clinical Trials

The Effect of Parenteral Nutrition Supplement on Esophagectomy Patients

Start date: July 2012
Phase: N/A
Study type: Interventional

Malnutrition is common in esophagus cancer patients, especially after surgery therapy. Whether parenteral supplement with enteral nutrtion is benificial for patients after esophagectomy is controversial, when compared with enteral nutrition alone. In this study, the investigators are to examine the effect of enteral nutrition supplemented with parenteral nutrtion on nutrition status after esophagectomy.

NCT ID: NCT01626001 Completed - Lung Cancer Clinical Trials

Imaging Study Compare 4DCT Image

Start date: July 2012
Phase: Phase 1
Study type: Interventional

The goal of this clinical research study is to learn about ways to possibly reduce scanning errors when using 4-dimensional computed tomography (4D CT) scans to check lung function in patients with esophageal or lung cancer.

NCT ID: NCT00660205 Completed - Gastric Cancer Clinical Trials

Venous Thromboembolism and Haemostatic Disturbances in Patients With Upper Gastrointestinal Cancer

GIVTE
Start date: February 2008
Phase: N/A
Study type: Observational

Cancer is a well known risk factor for venous thromboembolism (VTE) such as deep venous thrombosis (DVT) and pulmonary embolism (PE). Today we know that patients with adenocarcinomas of the gastro intestinal tract (GI-tract) often is in a hypercoagulable state. In our observational study we collect patients admitted to department with a tentative diagnosis of upper GI cancer including pancreas cancer and offer them flow doppler ultrasounds of both legs for diagnosis of DVT in the entire treatment time. The routine CT-scan of the chest is modified to diagnose PE. This will be compared with blood samples analysed for coagulation markers including D-dimer - a fibrinogen degradation product.