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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05141656
Other study ID # CPOG-CDPC-01
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date August 31, 2019
Est. completion date July 31, 2023

Study information

Verified date November 2021
Source RenJi Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is a multi-center observational study. The start time for data collection is August 31, 2019. Patients who have been treated at our institution from August 31, 2019, who were diagnosed with pancreatic tumors on or before August 31, 2019 (diagnosed in our hospital or outside hospitals) would all meet the inclusion conditions of the study and be considered enrollment. Patients' baseline and treatment data will be collected under informed concent. The combination of medical big data governance and the leading technology of the big data platform uses real world data to improve the quality and efficiency of pancreatic tumor diagnosis, treatment and scientific research.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20000
Est. completion date July 31, 2023
Est. primary completion date July 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: 1. Age = 18, both male and female; 2. Patients with primary pancreatic tumor diagnosed by histology, cytology or imaging; 3. Clinical or pathological staging is locally advanced or metastatic pancreatic tumor (newly diagnosed or after surgery and other treatments); 4. You can accept or have not received surgery, chemotherapy, radiotherapy, local treatment or traditional Chinese medicine for tumors; 5. The subject voluntarily joined the study and signed an informed consent form voluntarily. Exclusion Criteria: 1. Pancreatic tumors are evaluated as metastatic lesions, not primary tumors of the pancreas.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention will be considered in this study.
No intervention will be considered in this study.

Locations

Country Name City State
China RenJiH Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
RenJi Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary OS overall survival 5 years
Secondary DFS disease free survival 5 years
Secondary PFS progress free survival 5 years
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