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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06265311
Other study ID # 20221307-2
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 2, 2021
Est. completion date June 2024

Study information

Verified date February 2024
Source Shanghai Municipal Hospital of Traditional Chinese Medicine
Contact Hang Zhao, PhD
Phone 18621186288
Email drzhaohang@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to observed CBD stones cases with high recurrence risks applying IDUS or not during ERCP. Patients with CBD stone high recurrence risks were enrolled in this study, and prospectively randomized into IUDS group and control group during lithotomy. Operation time, radiation time, hospitalization cost, retain of nasobiliary tube, deployment of stent were recorded. Symptoms and conditions after ERCP were also followed up including blood amylase, routine blood test, abdominal pain, post-ERCP pancreatitis, resection of gallbladder, recurrence of CBD stone and onset of cholangitis.


Description:

Patients with CBD stone high recurrence risks were enrolled in this study, and prospectively randomized into IUDS group and control group during lithotomy. High risks were defined as diameter of CBD>1.5cm, number of calculi>2, and lithotripsy. Operation time, radiation time, hospitalization cost, retain of nasobiliary tube, deployment of stent were recorded. Symptoms and conditions after ERCP were also followed up including blood amylase, routine blood test, abdominal pain, post-ERCP pancreatitis, resection of gallbladder, recurrence of CBD stone and onset of cholangitis.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date June 2024
Est. primary completion date January 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - 1.Clinical diagnosis of common bile duct stones 2.At least one of the following, diameter of CBD>1.5cm, or number of calculi>2, or lithotripsy during ercp Exclusion Criteria: - 1. Clinical diagnosis of liver or biliary malignant tumor. 2. Clinical diagnosis of duodenal malignant tumor 3. Failure or unexpected termination of ERCP 4. Surgery history of gallbladder or bile duct.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
IDUS examination
for patients with high risks of bile duct stones recurrence using IDUS during ERCP

Locations

Country Name City State
China Shang General Hospital Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Municipal Hospital of Traditional Chinese Medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary recurrence of bile duct stone or cholangitis patients will be followed up for 48 weeks to record the recurrence of CBD stones or cholangitis 48 weeks
Primary need for a nasobiliary tube it's a Yes or No categorical variable to describe if the patient was placed a nasobiliary tube during ERCP 2 weeks
Primary need for stents it's a Yes or No categorical variable to describe if stents were deployed during ERCP 4 weeks
Secondary operation time the time from tracheal intubation to the end of ERCP was recorded intraoperative
Secondary radiation time radiation time of each patient was recorded 4 weeks
Secondary hospitalization cost hospitalization cost of each patient was recorded 8 weeks
Secondary Questionnaire of Symptoms and conditions after ERCP Questionnaire of symptoms and conditions after ERCP were recorded. Degree of abdominal pain and distension were recorded with a highest level of three points respectively. 8 weeks
Secondary White blood cell count Routine blood test 12 weeks
Secondary Red blood cell count Routine blood test 12 weeks
Secondary Platelet count Routine blood test 12 weeks
Secondary total bilirubin, direct bilirubin Liver function test 12 weeks
Secondary Liver function test (ALT, AST) 12 weeks
Secondary albumin Liver function test 12 weeks
Secondary total protein Liver function test 12 weeks
Secondary Gamma-glutamyl transferase (GGT) test Liver function test 12 weeks
Secondary An alkaline phosphatase (ALP) test Liver function 12 weeks
Secondary whether have a resection of gallbladder checklist whether the patient has a resection of gallbladder after ERCP 48 weeks
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