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Pancreatitis clinical trials

View clinical trials related to Pancreatitis.

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NCT ID: NCT02622854 Completed - Acute Pancreatitis Clinical Trials

Plasma Exchange vs Conservative Management in Non-severe Acute Hypertriglyceridemic Pancreatitis

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

To compare effectiveness in reducing triglycerides between daily plasma exchange and glucose+insulin infusion in patients with non-severe acute hypertriglyceridemic pancreatitis with mildly elevated triglycerides

NCT ID: NCT02602808 Completed - Acute Pancreatitis Clinical Trials

Study of Peripheral Blood Non-coding RNAs as Diagnosis and Prognosis Biomarker for Acute Pancreatitis

NCRNAP
Start date: December 2015
Phase:
Study type: Observational

It is important to identify patients with acute pancreatitis who are at risk for developing persistent organ failure early in the course of disease. The investigators evaluated whether peripheral blood non-coding RNAs, including microRNAs and long noncoding RNA (lncRNA), could serve as a good marker for detection of acute pancreatitis with persistent organ failure at early phase.

NCT ID: NCT02577640 Completed - Clinical trials for Chronic Pancreatitis

Dietary Soy Isoflavones In Chronic Pancreatitis

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

Dietary Soy Isoflavones in Chronic Pancreatitis: Investigating the Anti-inflammatory Effects of Food Innovation Science on Gastrointestinal Disease

NCT ID: NCT02567240 Completed - Clinical trials for Chronic Pancreatitis

Carbon Monoxide-Saturated Medium for Islet Isolation

Start date: January 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this study is to determine whether harvesting islets using carbon monoxide (CO)-saturated mediums can protect islet cell from death after autologous islet transplantation in patients with chronic pancreatitis.

NCT ID: NCT02563080 Completed - Acute Pancreatitis Clinical Trials

Pancreatic Exocrine Insufficiency in Acute Pancreatitis

APPEI
Start date: September 2015
Phase:
Study type: Observational [Patient Registry]

Severe pancreatitis induces more damage in the pancreas and might therefore result reduced exocrine function leading to the insufficiency. The aim of this prospective study is to investigate development of pancreatic exocrine insufficiency in patients recovering from first attack of moderately severe or severe acute pancreatitis.

NCT ID: NCT02543658 Completed - Acute Pancreatitis Clinical Trials

Neostigmine Treatment of Acute Pancreatitis Combined With Intra-abdominal Hypertension

Start date: September 1, 2015
Phase: Phase 2
Study type: Interventional

Acute pancreatitis(A) often complicated with Intra-abdominal Hypertension. After the onset of acute pancreatitis, capillary leakage causing ascites,upper gastrointestinal tract obstruction and paralytic ileus leading to an elevated IAP, severe IAH leads to ACS with high mortality. Neostigmine is an anti-cholinesterase drugs, can enhance intestinal peristalsis, promote flatus defecation. The aim of this study was to determine the effect of neostigmine on reducing abdominal pressure and clinical prognosis in patients with AP by promoting intestinal peristalsis and defecation.

NCT ID: NCT02497872 Completed - Clinical trials for Common Bile Duct Stones

Early Precut Versus Pancreatic Stent for Post-ERCP Pancreatitis

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

BACKGROUND: The most common complication of endoscopic retrograde cholangiopancreatography (ERCP) is pancreatitis. Precut sphincterotomy has been regarded as a risk factor. However, early precut may actually reduce post-ERCP pancreatitis risk. However, early precut as a preventive measure has not been compared to other preventive measures, such as pancreatic duct stent placement. AIM: To compare the efficacy of early precut sphincterotomy versus pancreatic duct stent placement in high-risk subjects undergoing ERCP. MATERIALS AND METHODS: This is a single-blinded, randomized trial that took place in two tertiary referral centers in Buenos Aires. ERCP subjects shall present at least one of the following risk factors: female sex, age less than 40 years, clinical suspicion of Sphincter of Oddi dysfunction, previous pancreatitis, common bile duct diameter of less than 8 mm. Only those who present a difficult biliary cannulation shall be randomized into two groups: those who receive early precut sphincterotomy or those in whom persistency of biliary cannulation is intended with subsequent pancreatic duct stent placement after cholangiography is achieved. The incidence of post-ERCP pancreatitis as well as other complications shall be compared.

NCT ID: NCT02497196 Completed - Pelvic Pain Clinical Trials

Neurophysiological Effects on tPCS and tDCS on Healthy Subjects and on Patients With Chronic Visceral Pain

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

This study investigates comparing the effects of transcranial Pulsed Current Stimulation and transcranial Direct Current Stimulation (tDCS) (Soterix ©) and their combination on neurophysiological outcomes on healthy subjects as well as on the clinical population for chronic visceral pain. The study also aims to evaluate the effects of these techniques on pain thresholds in healthy subjects as well as for chronic visceral pain patients.

NCT ID: NCT02487225 Completed - Clinical trials for Gallstone Pancreatitis

Pentoxifylline Treatment in Acute Pancreatitis (AP)

AP
Start date: May 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine the effects (good and bad) of giving a drug called pentoxifylline to patients with acute pancreatitis.

NCT ID: NCT02476760 Completed - Clinical trials for Diabetes Mellitus, Type 2

Incretin-based Drugs and Acute Pancreatitis

Start date: March 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether incretin-based drugs (used to treat type 2 diabetes) taken either alone or in combination with other anti-diabetic drugs are associated with an increased risk of acute pancreatitis (AP) compared to other combinations of oral hypoglycemic agents (OHA). The investigators will carry out separate population based cohort studies using administrative health databases in six jurisdictions in Canada, the US, and the UK. Cohorts will be defined by the initiation of a new anti-diabetic drug when incretin-based drugs entered the market, with follow-up until hospitalization for AP. The results from the separate sites will be combined to provide an overall assessment of the risk of AP in users of incretin-based drugs and by class of incretin-based drugs.