- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06887023
Clinicopathologic Characteristics, Progression, and Prognostic Analysis of IPNB
March 14, 2025 updated by: Meng Wang, The First Hospital of Jilin University
Clinicopathologic Characteristics, Progression, and Prognostic Analysis of Intraductal Papillary Neoplasm of Bile Duct
The main aim of this observational study is to understand the clinicopathological and prognostic information of IPNB, a rare tumor.
The participants have already received treatment during their previous routine medical management and took part in follow - up.
We will look into their survival information after previous medical visits and treatment.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
118
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Jililn
-
Changchun, Jililn, China, 130000
- The First Hospital of Jilin University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients diagnosed with IPNB from eight Chinese hospitals over a 10-year period
Description
Inclusion Criteria:
- IPNB with or without malignant transformation was confirmed by pathological examination
Exclusion Criteria:
- missing other essential clinical data
- coexisting malignant tumors of other digestive system organs
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
death
Time Frame: From January 2014 to June 2024
|
Died of various causes after treatment
|
From January 2014 to June 2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2024
Primary Completion (Actual)
January 15, 2025
Study Completion (Actual)
February 1, 2025
Study Registration Dates
First Submitted
March 14, 2025
First Submitted That Met QC Criteria
March 14, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 14, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-1244
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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