Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:43 PM
Ignite Modification Date:
2025-12-24 @ 1:43 PM
NCT ID:
NCT05289895
Eligibility Criteria:
Inclusion Criteria:
Sequence 1 (pathological specimens and information collection of pancreatic cancer patients):
1. Chinese patients, regardless of age and gender;
2. patients with pancreatic cancer confirmed by pathology;
3. Patients without a second primary tumor;
4. 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):
1. Chinese patients, regardless of age and gender;
2. 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;
3. Patients with pancreatic malignancy diagnosed by pathology;
4. Patients without a second primary tumor.
Sequence 3 (healthy subject samples and information collection)
1. Chinese healthy male or female, aged 18-45;
2. 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;
3. 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 Criteria:
Sequence 1 :
1. The quality of pathological specimens of patients can not meet the requirements of proteomics;
2. The researchers believe that patients who are not suitable for proteomic analysis.
Sequence 2:
1. patients with other malignant tumors (non pancreatic cancer metastasis).
2. hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody positive or syphilis antibody positive;
3. Pregnant or lactating women;
4. The researcher believes that it is not suitable to participate in this experiment.
Sequence 3:
1. Abnormalities of clinical significance judged by clinicians, including physical examination, vital signs examination, ECG or clinical laboratory examination results;
2. hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody positive or syphilis antibody positive;
3. 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;
4. Those vaccinated with active or attenuated vaccine within 1 month before screening or during the planned trial;
5. Pregnant or lactating women;
6. Those who have taken any drugs within the first 14 days;
7. The researcher believes that it is not suitable to participate in this experiment.
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT05289895
Study Brief:
Protocol Section:
NCT05289895