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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05433935
Other study ID # PCIPMN
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date December 31, 2033

Study information

Verified date January 2023
Source Zhejiang University
Contact Tingbo Liang, PhD
Phone +86 19941463683
Email liangtingbo@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a prospective, open large cohort study to explore biomarkers for detecting early carcinogenesis of IPMN.


Description:

This prospective study was designed to explore biomarkers for detecting early carcinogenesis of IPMN. This study intends to prospectively and continuously enroll IPMN patients, and regularly collect biological samples including blood, urine, feces and saliva. We aimed to detect biomarkers which can predict the carcinogenesis of IPMN by multi-omics. The primary endpoint is the predictive accuracy of biomarkers for IPMN malignant transformation. The probability of IPMN malignant transformation , rates of surgical resection and survival after surgery are secondary endpoints.


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date December 31, 2033
Est. primary completion date June 30, 2032
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 0 Years to 90 Years
Eligibility Inclusion Criteria: - clinically diagnosed as IPMN; - without other malignant tumor; - agree to sign informed consent. Exclusion Criteria: - with mental disorders which can affect cognition and cooperation; - with serious blood diseases or taking drugs that can affect peripheral blood

Study Design


Related Conditions & MeSH terms

  • Intraductal Papillary Mucinous Neoplasm
  • Neoplasms

Intervention

Other:
Observation
This is an observational study.

Locations

Country Name City State
China the First Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang

Sponsors (6)

Lead Sponsor Collaborator
Zhejiang University Huizhou Municipal Central Hospital, Meng Chao Hepatobiliary Hospital of Fujian Medical University, Second Affiliated Hospital of Nanchang University, Shengzhou People's Hospital, The Second Hospital of Hebei Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The accuracy of IPMN malignant transformation Up to 10 years
Secondary the probability of IPMN malignant transformation Up to 10 years
Secondary rates of surgical resection Up to 10 years
Secondary survival after surgery Up to 10-15 years
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