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Pancreatic Cancer clinical trials

View clinical trials related to Pancreatic Cancer.

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NCT ID: NCT02777463 Completed - Pancreatic Cancer Clinical Trials

The Prediction Using Diffusion MRI of the Response Evaluation in BRPC in NAT.

DIFFERENT
Start date: June 2016
Phase:
Study type: Observational [Patient Registry]

To investigate the correlation between pretreatment ADC value of diffusion MRI and pathologic response in patients with borderline resectable pancreatic carcinoma who undergo neoadjuvant therapy.

NCT ID: NCT02767752 Terminated - Pancreatic Cancer Clinical Trials

Gemcitabine and Capecitabine With or Without T-ChOS as Adjuvant Therapy for Patients With Resected Pancreatic Cancer

CHIPAC
Start date: November 2016
Phase: Phase 2
Study type: Interventional

This is a single center, randomized, double-blind, placebo-controlled phase II trial that will compare the efficacy of T-ChOS in combination with gemcitabine to gemcitabine alone as adjuvant treatment for 6 months in patients with surgically resected pancreatic adenocarcinoma.

NCT ID: NCT02756468 Recruiting - Pancreatic Cancer Clinical Trials

Procalcitonin Reveals Early Dehiscence in Pancreatic Surgery: the PREDIPS Study

PREDIPS
Start date: January 2015
Phase: N/A
Study type: Observational [Patient Registry]

Background. Pancreatic cancer surgery is associated with very high risk of postoperative morbidity and mortality. Anastomotic leak (AL) is one of the worst complications associated with relevant short and long-term sequelae. Procalcitonin (PCT) is a biomarker used to monitor bacterial infections and guide antibiotic therapy and has been shown to have better predictive value of AL after colorectal surgery than C-reactive protein (CRP) and white blood cell count (WBC). Purpose. The investigators designed a monocentric pilot study to test if PCT might be a sensitive and reliable marker of AL after pancreatic surgery

NCT ID: NCT02745847 Active, not recruiting - Pancreatic Cancer Clinical Trials

Re-irradiation With Stereotactic Body Radiotherapy for Relapsed Pancreatic Cancer

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

The safety and efficacy of re-irradiation with stereotactic body radiotherapy for relapsed pancreatic cancer will be evaluated.

NCT ID: NCT02745197 Withdrawn - Pancreatic Cancer Clinical Trials

A Study to See Whether a Nutritional Supplement is Beneficial for Patients With Pancreatic Cancer

Start date: May 2017
Phase: Phase 2
Study type: Interventional

This study evaluates a nutritional supplement in the treatment of pancreatic cancer in adults. Half of the participants will receive the nutritional supplement, while the other half will receive a placebo.

NCT ID: NCT02743975 Terminated - Pancreatic Cancer Clinical Trials

Near-infrared Image Guided Surgery in Pancreatic Adenocarcinoma

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

There is a need for better visualization of resection margins and detection of small tumor deposits during surgery for pancreatic cancer. Optical molecular imaging of pancreatic ductal adenocarcinoma associated biomarkers is a promising technique to accommodate this need. The biomarker Vascular Endothelial Growth Factor (VEGF-A) is overexpressed in pancreatic cancer tissue versus normal tissue and has proven to be a valid target for molecular imaging. VEGF-A can be targeted by the monoclonal antibody bevacizumab. Monoclonal antibodies can be labeled by the near-infrared (NIR) fluorescent dye IRDye800CW (800CW). The investigators hypothesize that bevacizumab-800CW accumulates in VEGF expressing cancer, enabling pancreatic cancer visualization using a NIR intraoperative camera system. In this pilot intervention study the investigators will determine the optimal dosage of bevacizumab-800CW (4,5 10, 25 or 50mg) to detect pancreatic cancer tissue intraoperatively.

NCT ID: NCT02734680 Recruiting - Pancreatic Cancer Clinical Trials

IORT Followed by CCRT or SBRT for Locally Advanced Pancreatic Cancer

IFCSLAPC
Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to find the best model of combination of intraoperative radiotherapy(IORT) and postoperative radiochemotherapy for pancreatic cancer.

NCT ID: NCT02723331 Active, not recruiting - Pancreatic Cancer Clinical Trials

Perioperative Therapy for Resectable and Borderline-Resectable Pancreatic Adenocarcinoma With Molecular Correlates

Start date: December 30, 2016
Phase: Phase 2
Study type: Interventional

The objective of this study is to estimate the R0 resection rate in patients with Resectable Pancreatic Ductal Adenocarcinoma (R-PDAC) as well as those with Resectable Pancreatic Ductal Adenocarcinoma (BR-PDAC) independently in response to neoadjuvant sequential therapy of combination nab-paclitaxel and gemcitabine followed by stereotactic body radiotherapy (SBRT).

NCT ID: NCT02722616 Terminated - Pancreatic Cancer Clinical Trials

Ultrasound Monitoring of Abdominal Soft Tissue

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

This research study is being done to collect data and analyze the motion of soft tissue in the abdomen (liver, pancreas, stomach and intestines) of people who have pancreatic and liver cancer as well as healthy volunteers. During the study researchers will look at the movement of organs in the abdomen that naturally occurs with breathing and with a bowel movement. This study will examine the differences between abdominal soft tissue motion in healthy volunteers and in cancer patients with the goal of developing a better way to manage and minimize the abdominal soft tissue motion. Accurate location of the tumor is very important in treatment delivery and reduction of toxicity.

NCT ID: NCT02720666 Completed - Pancreatic Cancer Clinical Trials

K-001 Treatment of Advanced Pancreatic Cancer: Clinical Trial of Monotherapy's Tolerability

Start date: January 2016
Phase: Phase 1
Study type: Interventional

This study is an open and single-center Phase I clinical research on patients with advanced pancreatic cancer, for evaluating their adverse reactions or tolerance to K-001, so as to determine the safe and reasonable dosage and dosing regimen.