Skip to content

Urgent ERCP Pancreatic Duct Stenting in the Treatment of Acute Gallstone Pancreatitis Combined with Acute Cholangitis or Biliary Obstruction and Its Efficacy and Impact on Inflammatory Factors

Urgent ERCP Pancreatic Duct Stenting in the Treatment of Acute Gallstone Pancreatitis Combined with Acute Cholangitis or Biliary Obstruction and Its Efficacy and Impact on Inflammatory Factors

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050322
Enrollment
Unknown
Registered
2021-08-26
Start date
2021-08-23
Completion date
Unknown
Last updated
2022-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute pancreatitis

Interventions

Pancreatic duct stent group:ERCP+pancreatic duct stent placement
Non-pancreatic duct stent group:ERCP

Sponsors

General Hosptal of NingXia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 70 years; 2.Onset time = 8 points or CRP >= 150 mg/L; 4.Meets the diagnostic criteria of acute biliary pancreatitis and acute cholangitis at the same time; 5.Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients who have previously undergone pancreatic surgery; 2.Pregnant or lactating women; 3.Acute development stage of chronic pancreatitis; 4.Patients with severe heart, lung, liver, kidney, or mental illness that affect the treatment effect of acute pancreatitis or cannot cooperate with the operator (heart function> grade III, acute myocardial infarction, chronic kidney disease creatinine clearance rate <40ml/min, chronic obstructive pulmonary disease requiring long-term oxygen therapy, Child-Pugh grade C liver function of chronic liver disease, immune disease or immunosuppressed state, and dying patients); 5.Patients who cannot tolerate ERCP for various reasons (e.g., contrast agent allergy, severe fundus esophageal varices; Upper gastrointestinal obstruction, ulceration, bleeding, etc.; Coagulation dysfunction or long-term oral anticoagulants); 6.Patients who need to take pancreatic toxic drugs (such as estrogen, azathioprine, mesalazine, morphine derivatives, prednisone, etc.) during the study period; 7.Patients with biliopancreatic system tumors affecting the therapeutic effect.

Design outcomes

Primary

MeasureTime frame
Incidence of infectious pancreatic necrosis;Inflammatory factors;

Secondary

MeasureTime frame
Length of hospital stay;Daily visual analogue scale pain score changes;Dosage of pain medication;Incidence of new complications;Mortality rate;Daily changes in sequential organ failure test scores;Oral feeding time;Application time of anti-pancreatin drugs;Intensive care unit length of stay and underlying reasons;Expenses during treatment (within and outside the insurance);Changes in inspection index;

Countries

China

Contacts

Public ContactWang Zuozheng

General Hosptal of NingXia Medical University

wangzuozheng2008@sina.com+86 13895009292

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026