Status:

UNKNOWN

Prognostic Biomarkers of Pancreatic Cancer Based on Proteomic Techniques

Lead Sponsor:

The Affiliated Hospital of Qingdao University

Conditions:

Proteomics

Pancreatic Cancer

Eligibility:

All Genders

Brief Summary

Sequence I (Retrospective study: proteomic analysis of pathological specimens and information collection of previous patients with pancreatic cancer) Sequence 2 (Non-interventional prospective study, ...

Detailed Description

Sequence 1 was a retrospective study, which collected pathological tissue samples (continuous cut white slices, 10 slices per case, 2 of which were HE stained slices) and clinical data (including clin...

Eligibility Criteria

Inclusion

  • Sequence 1 (pathological specimens and information collection of pancreatic cancer patients):
  • Chinese patients, regardless of age and gender;
  • patients with pancreatic cancer confirmed by pathology;
  • Patients without a second primary tumor;
  • The clinical diagnostic information to be collected within three months before sampling is relatively complete.
  • Sequence 2 (samples and information collection of patients with pancreatic cancer):
  • Chinese patients, regardless of age and gender;
  • Subjects must obtain informed consent and sign informed consent, indicating that they understand the purpose and procedure of this study and are willing to participate in the study;
  • Patients with pancreatic malignancy diagnosed by pathology;
  • Patients without a second primary tumor.
  • Sequence 3 (healthy subject samples and information collection)
  • Chinese healthy male or female, aged 18-45;
  • Subjects must obtain informed consent and sign informed consent, indicating that they understand the purpose and procedure of this study and are willing to participate in the study;
  • Physical examination, vital signs, laboratory examination (blood routine, blood biochemistry and urine routine), 12 lead ECG and other normal or abnormal persons without clinical significance

Exclusion

  • Sequence 1 :
  • The quality of pathological specimens of patients can not meet the requirements of proteomics;
  • The researchers believe that patients who are not suitable for proteomic analysis.
  • Sequence 2:
  • patients with other malignant tumors (non pancreatic cancer metastasis).
  • hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody positive or syphilis antibody positive;
  • Pregnant or lactating women;
  • The researcher believes that it is not suitable to participate in this experiment.
  • Sequence 3:
  • Abnormalities of clinical significance judged by clinicians, including physical examination, vital signs examination, ECG or clinical laboratory examination results;
  • hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody positive or syphilis antibody positive;
  • Those who have participated in other clinical trials of drugs and accepted clinical trials of drugs or devices for trial within the first three months;
  • Those vaccinated with active or attenuated vaccine within 1 month before screening or during the planned trial;
  • Pregnant or lactating women;
  • Those who have taken any drugs within the first 14 days;
  • The researcher believes that it is not suitable to participate in this experiment.

Key Trial Info

Start Date :

April 1 2022

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

December 30 2024

Estimated Enrollment :

220 Patients enrolled

Trial Details

Trial ID

NCT05289895

Start Date

April 1 2022

End Date

December 30 2024

Last Update

March 22 2022

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