Relationship of CP and AP

Sponsor
Changhai Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04670705
Collaborator
(none)
1,022
129

Study Details

Study Description

Brief Summary

The present study aimed to determine the prevalence of AP attacks before the diagnosis of CP and further identified the potential associated factors for AP episodes.

Condition or Disease Intervention/Treatment Phase
  • Other: patients' characteristics

Study Design

Study Type:
Observational
Actual Enrollment :
1022 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
The Prevalence of Acute Pancreatitis Episodes Among Patients With Chronic Pancreatitis and the Associated Factors
Actual Study Start Date :
Jan 1, 2010
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Oct 1, 2020

Outcome Measures

Primary Outcome Measures

  1. the occurrence of acute pancreatitis [Baseline (before the diagnosis of CP)]

    the presence and frequency of acute pancreatitis before diagnosis of CP

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Consequent patients with a diagnosis of CP between January 2010 to December 2015

  • informed consents provided

Exclusion Criteria:
  • autoimmune pancreatitis (AIP)

  • pancreatic cancer diagnosed within 2 years after the diagnosis of CP

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Changhai Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhuan Liao, Principal Investigator, Changhai Hospital
ClinicalTrials.gov Identifier:
NCT04670705
Other Study ID Numbers:
  • AP&CP
First Posted:
Dec 17, 2020
Last Update Posted:
Dec 17, 2020
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 17, 2020