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Pancreatitis clinical trials

View clinical trials related to Pancreatitis.

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NCT ID: NCT00953199 Completed - Pancreatitis Clinical Trials

Topical Pancreatic Duct Lidocaine for Prevention of Post-ERCP Pancreatitis

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if lidocaine is effective in reducing the incidence of post-ERCP pancreatitis.

NCT ID: NCT00915863 Recruiting - Clinical trials for Pancreatic Neoplasms

Evaluation of Isolated Roux-en-Y Reconstruction After Pancreaticoduodenectomy

Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the incidence of complications with the isolated Roux-en-Y reconstruction after pancreaticoduodenectomy in pancreatic tumor and periampullary tumor patients. A prospective randomized controlled trial was conducted to compare the incidence of complications with isolated Roux-en-Y reconstruction with those of Billroth-II-type reconstruction after pancreaticoduodenectomy.

NCT ID: NCT00909103 Completed - Clinical trials for Pancreatic Adenocarcinoma

Endoscopic Ultrasound Elastography in Pancreatic Masses

EUS-EG
Start date: June 2008
Phase: N/A
Study type: Observational

The aim of the study is to assess elastography during EUS examinations of focal pancreatic masses, and to consequently differentiate benign versus malignant pancreatic masses in a prospective multi-center design.

NCT ID: NCT00904865 Recruiting - Cholecystitis Clinical Trials

Single Port Access (SPA) Cholecystectomy Versus Standard Laparoscopic Cholecystectomy

Start date: February 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Background: Single port access surgery is a rapidly progressing surgical approach which allows performance of standard laparoscopic surgery through a single transparietal port instead of multiple port accesses. Objective: Demonstrate the validity of Single port access (SPA) cholecystectomy compared to multiple ports laparoscopic cholecystectomy. Hypothesis: SPA cholecystectomy is associated with decreased parietal and body image trauma compare to multiple ports laparoscopic cholecystectomy. SPA cholecystectomy should be associated with better cosmetic results, may improve postoperative recovery due to lower parietal pain. SPA cholecystectomy may also be associated with decreased rate of parietal complications as lower numbers of transparietal port are placed. Methods: All patients offered cholecystectomy, either SPA or multiport cholecystectomy, included in the study will have recognized biliary pathology for which formal indication cholecystectomy are recognized internationally. Surgical technique, either for SPA cholecystectomy or for multiple ports cholecystectomy, will be the same except, that one surgical technique is achieved through a single transparietal port and the other through multiple ports. Randomization will be performed before surgeries after patients have given their informed consent to the study. No specific test or cost will be necessitated by the study. Patients will be informed orally and will receive a short study summary, allowing them to give an informed consent. Endpoints: - Morbidity - Body image and Cosmetic results - Post-operative pain (opioid sparing effect) - Operative time - Hospital stay

NCT ID: NCT00894907 Completed - Acute Pancreatitis Clinical Trials

Early Goal-directed Volume Resuscitation in Severe Acute Pancreatitis

EAGLE
Start date: August 1, 2009
Phase: N/A
Study type: Interventional

Acute pancreatitis (AP) is a common disorder with rising incidence varying between 35 and 80 per 100,000 in Europe and the USA. About 15% of patients develop necrotizing pancreatitis (NP) with a mortality of up to 42% and frequently prolonged hospitalisation in the survivors. Despite a fulminant pathophysiology comparable to that of sepsis, the management of NP is still re-active, symptomatic and mainly based on paradigms with low grade evidence. In sepsis beneficial effects of early goal-directed fluid resuscitation resulting in reduced mortality have been clearly shown. With regard to these data and several studies of NP demonstrating the deleterious effects of fluid loss and haemoconcentration within the first 24h after admission, early goal-directed fluid resuscitation has the potential of improving outcome also in NP. Therefore, it is the aim of this RCT to demonstrate beneficial effects of early goal-directed resuscitation using an algorithm based on modern haemodynamic parameters such as Intra-thoracic Blood Volume Index (ITBI), Extravascular Lung Water Index (ELWI) and Stroke Volume Variation (SVV) which can be easily and safely obtained due to recent progress in haemodynamic monitoring. The algorithm is aimed at maintaining adequate resuscitation (ITBI, SVV) as well as preventing pulmonary over-hydration (ELWI).The use of a similar algorithm in cardiac surgery patients resulted in a significant reduction in catecholamine use, lactate levels, duration of ventilation and ICU stay.

NCT ID: NCT00863642 Completed - Clinical trials for Gallstone Pancreatitis

Early Versus Delayed Surgery for Gallstone Pancreatitis

Start date: November 2007
Phase: N/A
Study type: Interventional

While there exists consensus among surgeons that patients with gallstone pancreatitis should undergo cholecystectomy to prevent recurrence, the precise timing of laparoscopic cholecystectomy for mild to moderate disease remains controversial. We hypothesize that laparoscopic cholecystectomy performed within 48 hours of admission, regardless of resolution of abdominal pain or abnormal laboratory values, will result in a shorter hospital stay.

NCT ID: NCT00853515 Terminated - Acute Pancreatitis Clinical Trials

Goal-directed Fluid Resuscitation in Acute Pancreatitis

Start date: March 2009
Phase: N/A
Study type: Interventional

Vigorous fluid resuscitation is currently believed to play a key role in reducing complications associated with acute pancreatitis. However, aggressive fluid replacement can be associated with complications such as pulmonary fluid sequestration. The purpose of this study is to evaluate alternative approaches to early fluid resuscitation for patients with acute pancreatitis.

NCT ID: NCT00851955 Completed - Pancreatic Cancer Clinical Trials

Role of CXCR2 Ligands/CXCR2 Biological Axis in Pancreatic Cancer

Start date: May 2007
Phase: N/A
Study type: Observational

The investigators hypothesize that the CXCR2 ligands/CXCR2 biological axis plays an important role in promoting angiogenesis in PC; and that the genetic changes and the microenvironment of the tumor regulate the expression of CXCR2 ligands/CXCR2 in PC in order to potentiate their angiogenic phenotype. A corollary of this hypothesis is that the cell surface receptors (CXCR2) and the intracellular signaling pathways that mediate the angiogenic responses induced by ELR+ CXC-chemokines are potential targets for novel therapeutic interventions in PC.

NCT ID: NCT00820612 Terminated - Clinical trials for Post-ERCP Pancreatitis

Rectal Indomethacin in the Prevention of Post-endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis in High Risk Patients

Start date: January 2009
Phase: Phase 4
Study type: Interventional

Pancreatitis (inflammation of the pancreas) is the most common complication of endoscopic retrograde cholangiopancreatography (ERCP), a procedure for the diagnosis and treatment of disorders of the pancreas and bile duct. Preliminary data has shown that non-steroidal antiinflammatory drugs, when administered rectally, can reduce the risk of pancreatitis after ERCP. This study is intended to definitively determine whether rectally administered indomethacin (a non-steroidal antiinflammatory drug)is effective at preventing pancreatitis after ERCP.

NCT ID: NCT00793715 Recruiting - Mortality Clinical Trials

Laparotomy Versus Percutaneous Puncture in Patients With Abdominal Compartment Syndrome During Acute Pancreatitis

DECOMPRESS
Start date: July 2010
Phase: N/A
Study type: Interventional

Decompressive laparotomy with temporary abdominal closure, will decrease of overall mortality and major morbidity in patients with abdominal compartment syndrome during acute pancreatitis in comparison with percutaneous puncture with placement of abdominal catheter.