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Pancreatitis clinical trials

View clinical trials related to Pancreatitis.

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NCT ID: NCT03632616 Enrolling by invitation - Clinical trials for Chronic Pancreatitis

Quality of Life Assessment of Chronic Pancreatitis Endoscopic Interventions

QOLAPI
Start date: July 1, 2017
Phase:
Study type: Observational

This study seeks to evaluate the effect of endoscopic interventions on quality of life in patients with chronic pancreatitis. Quality of life will be evaluated using the PANQOLI, a validated quality of life instrument specific to chronic pancreatitis. Endoscopic interventions will include pancreatic duct dilation and stenting, celiac plexus block, lithotripsy and removal of pancreatic duct stones, and pseudocyst drainage.

NCT ID: NCT03629600 Completed - Clinical trials for Post-ERCP Acute Pancreatitis

Trial of Aggressive Hydration Versus Rectal Indomethacin for Prevention of Post-ERCP Pancreatitis

AHRI-PEP
Start date: October 15, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Endoscopic Retrograde Cholangiopancreatography (ERCP) is a commonly performed endoscopic procedure used to treat pancreato-biliary pathology. Acute pancreatitis or post-ERCP pancreatitis (PEP), is the most common major complication of ERCP, which is reported to occur in 2-10% of patients overall (ranging from 2-4% in low risk patients up to 8-40% in high-risk patients). Hydration is a mainstay of treatment for acute pancreatitis, independent of etiology. Aggressive hydration has also been shown to decrease incidence of PEP. Rectal NSAIDs, including Indomethacin, has a proven role in prevention of PEP. Though both aggressive hydration and rectal indomethacin are efficacious in preventing PEP, there is no head to head trial comparing the efficacy of these two therapeutic modalities. Thus, the aim is to determine whether aggressive intravenous peri-procedural hydration or high dose rectal indomethacin immediately after ERCP decrease the incidence of PEP. The investigator's hypothesis is that prophylactic treatment with aggressive intravenous hydration is not inferior to rectal indomethacin in preventing PEP.

NCT ID: NCT03610308 Completed - Clinical trials for Cholecystitis; Gangrenous

ESTES Snapshot Audit 2018

Start date: October 1, 2018
Phase:
Study type: Observational [Patient Registry]

To explore differences in patients, techniques and outcomes across the international cohort to identify areas of practice variability in the presentation and management of acute complicated calculous biliary disease.

NCT ID: NCT03609944 Recruiting - Pancreatitis Clinical Trials

SpHincterotomy for Acute Recurrent Pancreatitis

SHARP
Start date: September 27, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a procedure called Endoscopic Retrograde CholangioPancreatography (ERCP) with sphincterotomy reduces the risk of pancreatitis or the number of recurrent pancreatitis episodes in patients with pancreas divisum. ERCP with sphincterotomy is a procedure where doctors used a combination of x-rays and an endoscope (a long flexible lighted tube) to find the opening of the duct where fluid drains out of the pancreas. People who have been diagnosed with pancreas divisum, have had at least two episodes of pancreatitis, and are candidates for the ERCP with sphincterotomy procedure may be eligible to participate. Participants will be will be randomly assigned to either have the ERCP with sphincterotomy procedure, or to have a "sham" procedure. Participants will have follow up visits 30 days after the procedure, 6 months after the procedure, and continuing every 6 months until a maximum follow-up period of 48 months.

NCT ID: NCT03601325 Completed - Pancreatitis Clinical Trials

Acute Pancreatitis: Study of Possible Etiologies and Risk Factors Affecting Outcome

Start date: October 1, 2018
Phase:
Study type: Observational

This study is to assess the frequency of different etiologies of acute pancreatitis in our locality & assess the effect of different risk factors on outcome of the patients.

NCT ID: NCT03595150 Not yet recruiting - Clinical trials for Common Bile Duct Diseases

Diclofenac for Prevention of Post-ERC Pancreatitis

Start date: January 1, 2025
Phase: Phase 2/Phase 3
Study type: Interventional

The study aims at assessing the effectiveness of Diclofenac for prevention of post-ERCP pancreatitis. It will be undertaken embedded in the Swedish national register for Gallstone surgery and ERCP (GallRiks). Patients are randomised to Diclofenac prior to the ERCP or no prophylaxis. GallRiks is used to identify which patients fulfill the eligibility criteria and which patients develop pancreatitis after the ERCP.

NCT ID: NCT03568630 Recruiting - Clinical trials for Diabetes Mellitus, Type 2

Blood Markers of Early Pancreas Cancer

Start date: July 26, 2018
Phase:
Study type: Observational

Identifying biomarkers of early pancreatic ductal adenocarcinoma (PDAC) could facilitate screening for individuals at higher than average risk and expedite the diagnosis in individuals with symptoms and substantially improve an individual's chance of surviving the disease. The investigators propose a longitudinal study of subjects at higher than average risk of PDAC in order to generate clinical data and bank serial blood specimens.

NCT ID: NCT03566173 Completed - Acute Pancreatitis Clinical Trials

Association Between Nonalcoholic Fatty Liver Disease and Acute Pancreatitis

Start date: March 10, 2018
Phase:
Study type: Observational [Patient Registry]

The early evaluation of AP severity are vital. Previous studies have shown non-alcoholic fatty liver disease (NAFLD) is associated with severity of acute pancreatitis (AP). This study is aimed to investigate the relationship between NAFLD and AP severity.

NCT ID: NCT03561441 Completed - Pancreatitis Clinical Trials

Tailored Hydration for the Prevention of Post-ERCP Pancreatitis

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Aggressive hydration of lactated Ringer's solution has shown considerable beneficial effect in preventing post-ERCP(endoscopic retrograde cholangiopancreatography) pancreatitis. But the occurence rate of post-ERCP pancreatitis are near 10% and there are severe complications of aggressive hydration due to hypervolemia such pulmonary and peripheral edema, prolonged hospital stay and increased medical expense. Also there are no definite guidelines that suggest the duration and amount of hydration. This study evaluates the efficacy and safety of tailored hydration depending on each patient's condition that indicates the likelihood of developing post-ERCP pancreatitis.

NCT ID: NCT03547232 Recruiting - Acute Pancreatitis Clinical Trials

Rectal Indomethacin as Early Treatment for Acute Pancreatitis (INDOMAP Trial)

INDOMAP
Start date: June 1, 2024
Phase: Phase 4
Study type: Interventional

Acute pancreatitis (AP) is an inflammatory condition of the pancreas following the activated pancreatic enzymes induced by varied causes, with or without other organ(s) dysfunction. The production and release of inflammatory factors is generally considered as the key factor of pathogenesis. Non-steroidal anti-inflammatory drugs (NSAIDs) are the most commonly applied agents for inflammatory diseases. A series studies have proved that indomethacin can reduce the risk of post-endoscopic retrograde cholangiopancreatography (ERCP), but high-quality evidence is still lacking in the field of effectiveness of NSAIDs to treat, rather than prevent, other types of AP. Majority of animal experiments showed that NSAIDs had protective effects for organ functions, but the results of several preliminary clinical studies were inconsistent. Randomized controlled trials are eagerly awaited to elucidate its effects on AP.