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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06277414
Other study ID # 2024ll0204001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date December 31, 2024

Study information

Verified date February 2024
Source The First Affiliated Hospital of University of South China
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To develop effective preoperative and postoperative prediction models for postoperative complications of ERCP


Description:

To develop effective preoperative and postoperative prediction models for postoperative complications of ERCP based on machine learning


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Routine ERCP patients Exclusion Criteria: - Unwillingness or inability to consent for the study - Pregnant women or breastfeeding - current acute pancreatitis

Study Design


Related Conditions & MeSH terms

  • Endoscopic Retrograde Cholangiopancreatography

Intervention

Other:
collection of laboratory test results, imaging results and symptoms
collection of laboratory test results, imaging results and symptoms

Locations

Country Name City State
China The First Affiliated Hospital of University of South China Hengyang Hunan

Sponsors (1)

Lead Sponsor Collaborator
The First Affiliated Hospital of University of South China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants with Pancreatitis Typical abdominal pain, with the level of serum amylase increasing at least 3 times of the normal range within 24 hours after ERCP. 1 month
Secondary Number of Acute PEC(post-ERCP-cholecystitis ) Number of Acute PEC(post-ERCP-cholecystitis ) 1 month
Secondary Number of Participants with Cholangitis Temperature should be more than 38 celsius degree, chills, with right upper abdominal pain, blood routine showing the total amount of the White Blood Cell (WBC), and the amount of polymorphonuclear neutrophil(PMN) are above normal 1 month
Secondary Number of Participants with Perforation Typical abdominal pain,abdominal muscle tension, and there are also radiographic evidence suggesting 1 month
Secondary Number of Participants with bile duct stents If it is necessary to get the patients drainage, Number of Participants with stents or endoscopic nasobiliary drainage (ENBD) should be recorded 1 month
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Recruiting NCT03413111 - Modified Double Wire Technique to Facilitate the Successful Cannulation N/A
Terminated NCT03057769 - Effect of Papillary Epinephrine Spraying on Post-ERCP Pancreatitis in Patients Received Rectal Indomethacin N/A
Recruiting NCT01745978 - Compare the Knob-tipped Knife With the Needle Knife in Difficult Biliary Cannulation Phase 3