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Pancreatic Tumor clinical trials

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NCT ID: NCT02269683 Withdrawn - Pancreatic Tumor Clinical Trials

Robotic vs. Laparoscopic Distal Pancreatectomy for Pancreatic Cancer

DAVID
Start date: n/a
Phase: N/A
Study type: Interventional

The present randomized controlled trial evaluates the incidence of R1 resections in patients undergoing robotic distal pancreatectomy compared to the laparoscopic technique.

NCT ID: NCT01978808 Recruiting - Pancreatic Tumor Clinical Trials

Efficiency Study of the EUS-FNA Needles With and Without a Side Port in Pancreatic Masses

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

For diagnosis of pancreatic tumors, endoscopic ultrasound (EUS) and EUS-guided fine needle aspiration (EUS-FNA) are well established techniques in clinical practice. We hypothesize that a FNA needle with a side port could improve the diagnostic yield. The aim of this prospective randomized study is to determine whether there is a difference in diagnostic yield in patients with pancreatic masses for evaluation.

NCT ID: NCT01969110 Recruiting - Pancreatic Tumor Clinical Trials

Additional Effects of Perioperative Immunonutrition in Patients Undergoing Pancreaticoduodenectomy

Start date: January 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate whether perioperative immunonutrition has additional effects on cell-mediated immunity in patients undergoing pancreaticoduodenectomy.

NCT ID: NCT01819961 Not yet recruiting - Liver Tumor Clinical Trials

Parenteral Fish Oil in Major Laparoscopic Abdominal Surgery

Start date: April 2013
Phase: Phase 4
Study type: Interventional

The aim of this study is to assess the effect of postoperative parenteral fish oil on clinical outcome and immune function after major laparoscopic abdominal surgery.

NCT ID: NCT01698190 Recruiting - Lymphadenopathy Clinical Trials

Comparing the Efficacy of Endoscopic FNA vs FNB in Diagnosing Solid Gastrointestinal Lesions

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

The purpose of this study is to determine if fine needle aspiration or fine needle biopsy is more efficacious and cost-effective than the other while maintaining diagnostic accuracy in the setting of solid gastrointestinal lesions.

NCT ID: NCT01692873 Completed - Pancreatic Tumor Clinical Trials

Prognostic and Predictive Biomarkers of Therapeutic Response in Pancreatic Tumors

PACAomics
Start date: February 2012
Phase: N/A
Study type: Interventional

Pancreatic cancer is among the most serious human neoplasia and the most difficult to treat. Most patients present at diagnosis a non resectable, locally advanced or metastatic disease, with a median survival of 12 month. The aim of this study is the identification of diagnosis biomarkers, predictive of the therapeutic response. This project investigate the use of molecular analyses applied to pancreatic tumor cells collected by microbiopsy under ultrasound-endoscopy, and blood cells.

NCT ID: NCT01673334 Completed - Pancreatic Tumor Clinical Trials

Evaluation of EUS-Guided 22 Gauge Core Biopsy Versus Fine-needle Aspiration for Suspected Pancreatic Neoplasms

Start date: September 2011
Phase: Phase 4
Study type: Interventional

We aim to compare the efficacy (diagnostic yield), ease of use, and technical success rates of EUS guided 22 gauge fine needle aspiration to core biopsy in the evaluation of pancreatic tumors. The experimental hypothesis is that FNA will have superior overall diagnostic yield than core biopsy.

NCT ID: NCT01479803 Completed - Pancreatic Tumor Clinical Trials

Comparison of Two Needles (ProCore vs EchoTip) for the Diagnosis of Pancreatic Solid Mass Under EUS

PICORE
Start date: October 2011
Phase: Phase 3
Study type: Interventional

The negative predictive value of fine needle aspiration under ultrasound endoscopy (EUS) for the diagnostic of solid pancreatic masses is 70% on average in the current literature with 22 gauge needles. There is a wide variability of this rate across studies (from 38 to 92%). In case of negativity of the biopsy, the risk of missing a pancreatic cancer whose prognosis is severe and extensive treatment, remains important. To improve the sensitivity of EUS echo endoscopy, several methods were used. A new needle (Echo Tip ® HD ProCore ™) has received CE Mark in the field of EUS. This instrument combines the comfortable and handy size of 22 Gauge and innovative design (window lateralized bevel) with in vitro studies obtaining core biopsy. In addition, a single pass through the tumor is achieved with this hand against several (2-3 minimum) with the current hardware. The theoretical goal is to have a tissue material more abundant during the sampling, without increasing morbidity and increase the diagnostic accuracy. A preliminary prospective study with this material has shown interesting results (increase the diagnostic accuracy of 15%). To determine the diagnostic gain with this new hand, it seemed essential to propose a prospective comparative study (22 gauge needle ProCore ™ versus the old EchoTip ® 22-Gauge) randomized (randomization of the order of the needles) in crossover (on the same lesion) in samples of pancreatic solid tumors. The caliber of 22 gauge is the gauge most often used for punctures under ultrasound endoscopy, resulting in less morbidity. Puncture by the 2 needles on the same injury can limit the effect of variability between patients and thereby have a better power for the investigators study without increasing the risk of complications (the needle ProCore ™ does not require that one pass through the tumor). The study of pancreatic solid tumors is one that poses the biggest diagnostic problem still present in the investigators daily practice. The aim of this study is to compare the diagnostic accuracy of the needle ProCore™ versus EchoTip® in etiological cyto histological diagnostic for pancreatic solid tumors under EUS.

NCT ID: NCT01434550 Withdrawn - Pancreatic Tumor Clinical Trials

Phase II Study of First-line SBRT in Patients With Non-Metastatic Unresectable Pancreatic Cancer

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

The purpose of this study is to see if SBRT will be a better way to treat pancreas cancer and to find out what effects, good and/or bad, this treatment will have on participants and their cancer.