跳至主要内容
临床试验/NCT03595150
NCT03595150尚未招募2 期

Diclofenac for Prevention of Post-ERC Pancreatitis

Karolinska Institutet0 个研究点目标入组 1,000 人开始时间: 2026年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
1,000
主要终点
Post-ERCP pancreatitis

研究概览

简要总结

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.

详细描述

Endoscopic Retrograde Cholangiopancreatography (ERCP) is a procedure commonly performed for diagnosing changes in the bile ducts or managing outflow obstruction. Although ERCP may in most cases be performed safely, there is a risk of developing acute pancreatitis following the procedure. The risk has been estimated to 5-10%, with an increased risk in women, younger patients and in case the cannulation is difficult.

Phospholipase 2 is crucial in the pathogenesis of acute pancreatitis. As Diclofenac is a potent inhibitor of Phospholipase 2, it has been suggested that it may be used for prevention of post-ERCP pancreatitis. There is some evidence for the effectiveness of Diclofenac, but more studies are needed to confirm that it reduces the risk of post-ERCP pancreatitis.

In order to test whether Diclofenac reduces the risk for post-ERCP pancreatitis, a register-based randomized controlled study is planned. The study will be conducted embedded in the Swedish Register for Gallstone Surgery and ERCP (GallRiks). GallRiks includes data corresponding to the eligibility criteria as well as outcome measures. GallRiks will also be used to record which patients have been screened for inclusion.

Patients who meet the eligibility criteria are invited to the study. If they accept inclusion, they are randomized to 100 mg Diclofenac prior to the ERCP or np prophylaxis. No blinding is done.

The aim is to include 1000 patients. When 500 patients have been included, an interim analysis will be performed, comparing the incidence of pancreatitis and mortality in the two groups. A retrospective review of the patient records will be performed for those who develop pancreatitis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing ERCP

排除标准

  • Decision to perform ERCP taken intraoperatively
  • Intolerance/allergy against NSAID
  • Patients taking NSAID daily
  • Severe cardiac fail (ASA>4)
  • Kidney failure (GFR<30 ml/min)
  • Coagulation disorder
  • History of peptic ulcer bleeding
  • History of abdominoperineal resection
  • Pregnancy
  • Patients who do not understand Swedish

研究组 & 干预措施

Diclofenac

Active Comparator

100 mg Diclofenac rectally prior to the ERCP

干预措施: Diclofenac (Drug)

结局指标

主要结局

Post-ERCP pancreatitis

时间窗: Within 30 days post-ERCP

Acute pancreatitis recorded in GallRiks by responsible endoscopist or surgeon. According to GallRiks criteria pancreatitis includes elevated amylase and abdominal pain of an intensity that hospital stay is warranted.

次要结局

  • Adverse drug reactions(Within 30 days post-ERCP)
  • Mortality(Within 30 days post-ERCP)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gabriel Sandblom

Associate Professor, Senior Consultant

Karolinska Institutet

相似试验