- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05088161
Prognostic Biomarkers of Pancreatic Cancer Based on Proteomics Techniques
October 19, 2021 updated by: The Affiliated Hospital of Qingdao University
In this study, we will use high-throughput proteomics techniques to search for biomarkers of post-operative prognosis of pancreatic cancer in samples of patients who have been diagnosed with pancreatic cancer through bioinformatics analysis.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This study plan from the affiliated hospital of Qingdao university collected 20 cases of patients with pancreatic cancer pathological tissue samples and clinical data, including clinical diagnostic information, laboratory tests, imaging examination results and other information data), through high-throughput proteomic technology in pancreatic cancer pathological finding biomarkers, the bioinformatics analysis to explore the prognosis biomarkers.
Study Type
Observational
Enrollment (Anticipated)
20
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yu Cao, Doctor
- Phone Number: 86-18661809090
- Email: caoyu1767@126.com
Study Locations
-
-
Shandong
-
Qingdao, Shandong, China, 266003
- Recruiting
- Phase I Clinical Research Center
-
Contact:
- Yu Cao, Doctor
- Phone Number: 86-18661809090
- Email: caoyu1767@126.com
-
-
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The subjects in this study were all patients with pathologically diagnosed pancreatic cancer.
Description
Inclusion Criteria:
- Patients of Chinese nationality, age and gender are not limited.
- Pathologically confirmed pancreatic cancer patients.
- Pathological specimens were archived tumor tissue samples after a diagnosis of pancreatic cancer.
- Clinical diagnostic information was complete three months before sampling.
Exclusion Criteria:
- Patients with a second primary tumor.
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 |
|---|---|---|
|
Differentially expressed proteins in tumor and paracancer tissues
Time Frame: 180 Days
|
Two dimensional gel electrophoresis, mass spectrometry and other techniques were used to separate and compare pancreatic cancer tissues and normal adjacent tissues to search for differentially expressed proteins.
|
180 Days
|
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)
May 13, 2021
Primary Completion (ANTICIPATED)
November 12, 2021
Study Completion (ANTICIPATED)
March 12, 2022
Study Registration Dates
First Submitted
June 23, 2021
First Submitted That Met QC Criteria
October 19, 2021
First Posted (ACTUAL)
October 21, 2021
Study Record Updates
Last Update Posted (ACTUAL)
October 21, 2021
Last Update Submitted That Met QC Criteria
October 19, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- JJDB-SR-2021-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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