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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05464303
Other study ID # ERBAAC
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 15, 2022
Est. completion date December 31, 2022

Study information

Verified date July 2022
Source Nanjing Children's Hospital
Contact Xie Hua, Dr
Phone +8613611573952
Email xiehua3955@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cholangitis is the most common postoperative complication of biliary atresia, with a reported incidence of 40-90%, which seriously affects the surgical effect, survival rate and the quality of life and prognosis of patients. Without of direct evidence, the diagnosis of cholangitis sometimes is difficult to make, thus most of them are diagnosed based on the symptoms of children. According to literature reports, different centers and regions have different diagnostic criteria for postoperative cholangitis after hepatic portoenterostomy, which has a great influence on the accuracy of the incidence rate and appropriate treatment of cholangitis, and also brings differences in the analysis of the causes and prognostic factors of cholangitis. Based on the above reasons, we used the Delphi method,in which worldwidely 48 experts participated in, to establish the diagnostic scoring system for postoperative cholangitis after biliary atresia. Now we aimed to verify the specificity and sensitivity of the new scoring system through clinical cases, in order to unify and standardize the diagnostic criteria and provide help for the diagnosis and treatment of cholangitis after biliary atresia.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group N/A to 16 Years
Eligibility Inclusion Criteria: ? Admission time: 2019.01.01-2021.12.31; ? The first diagnosis after discharge was cholangitis Exclusion Criteria: ? Cholangitis after non-Kasai procedure; - Postoperative cholangitis of biliary atresia not operated in the unit; ? Patient has been treated in other hospitals during this episode; ? The treatment period for cholangitis is not completed or the patient is discharged automatically.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Intravenous Antibodies
Treatment is usually performed with sensitive third-generation cephalosporins, and medication is adjusted according to blood culture results

Locations

Country Name City State
China NJMU Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Nanjing Children's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic cholangitis score The values of the two groups' scores were calculated separately Two years
Secondary Score estimates for treatment of cholangitis In the cholangitis group, the correlation between evaluation score and treatment was studied Two years
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