Safety and Efficacy of Extracorporeal Shock Wave Lithotripsy for Pancreatic Stones

Sponsor
Changhai Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05916547
Collaborator
(none)
2,500
1
1.1
2174.1

Study Details

Study Description

Brief Summary

To determine the types, incidence and risk factors of adverse events after pancreatic extracorporeal shock wave lithotripsy (P-ESWL), define the grading criteria of adverse events after P-ESWL, and analyze the efficacy of P-ESWL, which will provide evidence-based medical evidence to guide physicians' clinical practice.

Condition or Disease Intervention/Treatment Phase
  • Procedure: pancreatic extracorporeal shock wave lithotripsy

Detailed Description

Currently, pancreatic extracorporeal shock wave lithotripsy (P-ESWL) has become the preferred treatment for pancreatic duct stones. Although some studies had confirmed the safety and efficacy of P-ESWL, the sample size were small and the follow-up period were short. Therefore, investigators designed this study with a large sample and a long follow-up period to clarify the efficacy and safety of P-ESWL, so as to guide clinical work, standardize the diagnosis and treatment process of adverse events.

Study Design

Study Type:
Observational
Anticipated Enrollment :
2500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Safety and Efficacy of Extracorporeal Shock Wave Lithotripsy for Pancreatic Stones
Actual Study Start Date :
Jun 27, 2023
Anticipated Primary Completion Date :
Jul 26, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Outcome Measures

Primary Outcome Measures

  1. the incidence of post-ESWL adverse events [1 months]

    An adverse event of P-ESWL is classified as either a complication or a transient adverse event (TAE), depending on severity. Complications are recognized as adverse events needing specific medical intervention and prolonged hospitalization, while TAEs are defined as transient injuries caused by shock waves, which required no medical intervention and do not prolong hospitalization.

Secondary Outcome Measures

  1. the rate of pancreatic duct clearance [1 week]

    Complete clearance: more than 90% clearance of stone volume; partial clearance: 50% to 90% clearance of stone volume; unsuccessful clearance: failure to fragment the stones to less than 3 mm diameter or less than 50% clearance of stone volume.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients hospitalized in Changhai Hospital from 2011.02.01 to 2018.06.30.

  • Painful patients with chronic pancreatitis.

  • Patients who completed pancreatic extracorporeal shock wave lithotripsy.

Exclusion Criteria:
  • Patients who diagnosed pancreatic cancer within 2 years after diagnosing chronic pancreatitis.

  • Patients who refused to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Changhai Hospital Shanghai China 200433

Sponsors and Collaborators

  • Changhai Hospital

Investigators

  • Principal Investigator: Liang-hao Hu, MD, Changhai Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Zhaoshen Li, Professor, Changhai Hospital
ClinicalTrials.gov Identifier:
NCT05916547
Other Study ID Numbers:
  • SEEPS
First Posted:
Jun 23, 2023
Last Update Posted:
Jun 29, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Zhaoshen Li, Professor, Changhai Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2023