Aggressive Intravenous Hydration With Lactated Ringer's Solution for Prevention of Post-ESWL Pancreatitis

NCT05772234 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1066

Last updated 2025-03-28

No results posted yet for this study

Summary

The goal of this clinical trial is to clarify whether aggressive intravenous hydration with lactated Ringer's solution could reduce the incidence of post-ESWL pancreatitis in patients with chronic pancreatitis.

Conditions

  • Pancreatitis, Chronic
  • Pancreatic Duct Stone

Interventions

DRUG

Lactated ringers solution

Intravenous 20 mL/kg Ringer's lactate solution within 60 min from the start of ESWL, directly followed by 3 mL/kg per h for 8 h.

DRUG

normal saline

Intravenous fluid infusion with normal saline (maximum of 1.5mL/kg per h or 3L per 24h).

Sponsors & Collaborators

  • Ruijin Hospital

    collaborator OTHER
  • LanZhou University

    collaborator OTHER
  • First People's Hospital of Hangzhou

    collaborator OTHER
  • The Second Affiliated Hospital of Baotou Medical College

    collaborator OTHER
  • Shanghai Pudong New Area Gongli Hospital

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Qilu Hospital of Shandong University

    collaborator OTHER
  • The Third Xiangya Hospital of Central South University

    collaborator OTHER
  • Affiliated Hospital of Yunnan University

    collaborator OTHER
  • Changhai Hospital

    lead OTHER

Principal Investigators

  • Lianghao Hu, M.D. · Changhai Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-17
Primary Completion
2025-03-18
Completion
2025-03-23

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05772234 on ClinicalTrials.gov