Endoscopic and shockwave therapy for painless chronic pancreatitis
Official title: Endotherapy and/or Extracorporeal Shockwave Lithotripsy Versus Conservative Treatment in Painless Chronic Pancreatitis
Run by Changhai Hospital · NCT07074379 · Data updated 2026-11-12
This study will test whether endoscopic duct procedures and/or shockwave lithotripsy help adults with painless chronic pancreatitis who have not had these treatments before improve pancreatic function and related symptoms.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 85 Years |
| Sex | All |
| Enrollment | 126 (estimated) |
| Sponsor | Changhai Hospital Academic / other |
| Locations | 1 site (Shanghai, Shanghai Municipality) |
| Status | Recruiting |
| Started | July 21, 2025 |
| Main results expected | December 1, 2027 |
| Study ends | July 1, 2037 |
| Registry record updated | September 23, 2026 |
| Trial ID | NCT07074379 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18–85 diagnosed with painless chronic pancreatitis who have not previously undergone ERCP or ESWL and who do not have surgical complications or contraindications are ideal candidates.
✕Probably not a fit
Patients with complications that require surgery, autoimmune pancreatitis, suspected cancer, prior pancreatic surgery, end-stage disease, pregnancy, or contraindications to ERCP/ESWL are unlikely to benefit from enrollment.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study enrolls adults aged 18–85 with painless chronic pancreatitis and no prior ERCP or ESWL to receive standard medical care plus endoscopic retrograde cholangiopancreatography (ERCP) and/or extracorporeal shockwave lithotripsy (ESWL) as indicated. Participants may also receive lifestyle advice, pancreatic enzyme replacement, and antidiabetic medications according to clinical need. Key exclusions include complications requiring surgical intervention, autoimmune pancreatitis, suspected malignancy, prior pancreatic or gastrointestinal bypass surgery, end-stage disease, pregnancy, and contraindications to ERCP/ESWL. The study is conducted at Changhai Hospital in Shanghai and compares clinical outcomes following these interventions in the painless CP population.
Why it matters
Potential benefit: If successful, the treatments could improve pancreatic duct clearance and help preserve or improve endocrine and exocrine pancreatic function in people with painless chronic pancreatitis.
How similar studies have gone: ERCP and ESWL have shown benefit for stone clearance and pain relief in obstructive or painful chronic pancreatitis, but their specific benefit in the painless chronic pancreatitis subgroup is less well studied.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 18-85 years. * Diagnosed with painless chronic pancreatitis. * No prior history of endoscopic retrograde cholangiopancreatography (ERCP) or extracorporeal shockwave lithotripsy (ESWL) treatment. * Stone(s) in the cephalic or corporeal portion of the main pancreatic duct with upstream duct dilation Exclusion Criteria: * Presence of complications requiring endoscopic or surgical intervention, such as pancreatic pseudocysts, benign biliary strictures, pancreatic fistulas, or pancreatic portal hypertension. * Autoimmune pancreatitis. * Suspected malignancy. * History of pancreatic surgery or gastrointestinal bypass surgery (e.g., Billroth II procedure). * End-stage disease. * Pregnancy or lactation. * Contraindications to ESWL or ERCP. * Refusal to provide informed consent.
Where it's running
-
Changhai Hospital
Shanghai, Shanghai Municipality, China Recruiting
Study contacts
- Study coordinator: Zhao-Shen Li
- Email: zhaoshen-li@hotmail.com
- Phone: +8613901960921
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.