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Pancreatic Neoplasms clinical trials

View clinical trials related to Pancreatic Neoplasms.

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NCT ID: NCT02911974 Completed - Pancreatic Neoplasm Clinical Trials

Comparing Biopsy Needles for Endoscopic Ultrasound Guided Samples for Pancreatic Masses

Expect
Start date: August 2016
Phase: N/A
Study type: Interventional

This is a randomized prospective clinical study comparing a fine needle biopsy device and an aspiration needle.

NCT ID: NCT02910960 Completed - Pancreatic Neoplasm Clinical Trials

Comparison of Two Fine Needle Biopsy Needles for Solid Pancreatic Masses

Expect
Start date: December 2016
Phase: N/A
Study type: Interventional

This is a randomized prospective clinical study comparing the Acquire Biopsy Device to SharkCore Biopsy Device.

NCT ID: NCT02909530 Completed - Clinical trials for Pancreatic Neoplasms

Comparison Between Olympus EZ Shot 3Plus 19G and EZ Shot 2 19G in EUS-guided FNB of Solid Pancreatic Masses

Start date: September 2016
Phase: N/A
Study type: Interventional

Endoscopic ultrasound-guided fine needle biopsy (EUS-FNB) is a valid and recommended technique for tissue diagnosis of pancreatic masses. However, the diagnostic yield is with a sensitivity of 64%-95% and an accuracy of 78%-94% still very low. The EUS-FNB of pancreatic masses is usually performed with a 22-gauge biopsy needle. The small diameter of the needle is usually responsible for the low yield of tissue samples for histopathological examination. The 19-gauge needles help to overcome the limitations of a 22-gauge needle by acquiring a larger amount of cellular material. Thus, performing EUS-FNB with a 19-gauge needle can maximize tissue acquisition and sample adequacy, which is important for appropriate diagnosis. Contrariwise, the technical success rate for sample retrieval in patients with pancreatic head lesions is significantly lower using the 19-gauge compared to the 22-gauge needle. This is attributable to the technical difficulty to push the needle out of the endoscope in the duodenum. Since about 60% of pancreatic cancers are located in the head region, it is therefore particularly important to improve technical success in these cases. The new 19-gauge biopsy needle "Olympus EZ Shot3 Plus" is more flexible than common biopsy needles such as "EZ Shot2" and should therefore provide improved access to regions like pancreatic head. The aim of this multicenter prospective randomized crossover study is to compare those two needles during EUS-FNB of solid pancreatic masses. Therefore this study will enroll 40 patients in five German centers with solid pancreatic masses and consecutive indication for EUS-FNB. Both needles will be used in each patient following a predetermined random order. Primary endpoint is the correct histological diagnosis of the mass assessed by each needle. Technical failure is regarded as a negative histological diagnosis. Secondary endpoints include a comparison of technical failure using each needle, histological quality, duration of procedure and rate of adverse events.

NCT ID: NCT02909296 Completed - Pancreatic Cancer Clinical Trials

Endoscopic Drainage of Collections After Pancreatic Surgery

COLLECTOR
Start date: April 2007
Phase: N/A
Study type: Observational

The pancreatic surgery causing some pancreatic collections. And in a number of case, this surgery can require a surgical resumption, a percutaneous drainage or an endoscopic drainage. The endoscopic care of the treatment of pancreatic collections post-surgery is not yet standardized. After failure of the medical treatment, the drainage of collections by echo-endoscopy was described. There are not much series on this specific subject. Only 2 series contain more than 20 patients with 31 patients for the most important. The timing and the technical choice of the endoscopic treatment as well as the long-term follow-up are not clear. The purpose of this study is to estimate the success and the complications of the endoscopic drainage by echo-endoscopy according to the techniques of drainage and the timing of the endoscopic treatment. The not estimated long-term follow-up will be also considered.

NCT ID: NCT02907099 Completed - Clinical trials for Metastatic Pancreatic Adenocarcinoma

Pembrolizumab and CXCR4 Antagonist BL-8040 in Treating Patients With Metastatic Pancreatic Cancer

Start date: December 1, 2016
Phase: Phase 2
Study type: Interventional

This pilot phase IIb trial studies how well pembrolizumab and CXCR4 antagonist BL-8040 work in treating patients with pancreatic cancer that has spread to other places. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. CXCR4 antagonist BL-8040 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving pembrolizumab and CXCR4 antagonist BL-8040 may work better in treating patients with pancreatic cancer.

NCT ID: NCT02905578 Active, not recruiting - Pancreas Cancer Clinical Trials

A Phase 2 Trial of High-dose Ascorbate for Pancreatic Cancer (PACMAN 2.1)

Start date: November 28, 2018
Phase: Phase 2
Study type: Interventional

This clinical trial adds high-dose ascorbate (vitamin C) to the standard of care regimen for metastatic pancreatic adenocarcinoma (a type of pancreatic cancer). Subjects are randomized between a control group (standard treatment) and an intervention group (pharmacologic ascorbate in addition to the standard treatment).

NCT ID: NCT02902484 Terminated - Cancer of Pancreas Clinical Trials

Study of Nintedanib and Chemotherapy for Advanced Pancreatic Cancer

Start date: September 7, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The study will perform a clinical study evaluating the safety and tolerability of nintedanib when combined with standard chemotherapy (Gemcitabine + nab-Paclitaxel) for metastatic pancreatic cancer. It will utilize advanced imaging correlates including dynamic contrast enhanced Magnetic Resonance Imaging (DCE-MRI) which correlates with tumor grade and microvessel density.

NCT ID: NCT02900950 Completed - Pancreatic Neoplasm Clinical Trials

Multicolour Versus Monocolour Specimens Inking After Pancreaticoduodenectomy for Periampullary Cancer

MPM
Start date: June 2012
Phase: N/A
Study type: Interventional

A single-centre, randomised clinical trial of patients affected by periampullary cancer who underwent pancreaticoduodenectomies which included two different types of specimen margination: arm A (multicolour inking) and arm B (monocolour inking). The randomisation of the specimen was made after the resection, blinded for the surgeons involved in the operation. The primary endpoint was the overall R1 resection rate and its difference between the two arms. The secondary endpoints were the R1 resection rate in each margin and its difference between the two arms, and the impact of margin status on survival. A sample size of 18 patients was required.

NCT ID: NCT02900677 Recruiting - Pancreatic Cancer Clinical Trials

Developing Prehabilitation Program in Patients With Operable Pancreatic Cancer Perioperatively and Following Surgery

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

The aims of this three-year study are to: 1. explore the change of fatigue, nutritional status, quality of life and care needs in patients with operable pancreatic cancer perioperatively and following surgery within 3 months. 2. develop and evaluate the effect of patient-centered cancer prehabilitation care program on improving fatigue, nutritional status and quality of life (QOL) in this population.

NCT ID: NCT02900248 Terminated - Multiple Myeloma Clinical Trials

CureOne Registry: Advanced Malignancy or Myelodysplasia, Tested by Standard Sequencing and Treated by Physician Choice

N1
Start date: October 2, 2017
Phase:
Study type: Observational [Patient Registry]

Registry participants with advanced malignancy or myelodysplasia will have a sample of their tumor or tissue analysed for genetic alterations using next generation sequencing (NGS) performed in a lab that has been certified to meet a high quality standard. Treatments and outcomes will be reported to the registry to allow further understanding of how genetic differences can lead to better diagnosis and treatments.