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 @ 10:06 PM
Ignite Modification Date:
2025-12-24 @ 10:06 PM
NCT ID:
NCT01526135
Eligibility Criteria:
Inclusion Criteria:
1. Histologically proven pancreatic ductal adenocarcinoma. Intraductal papillary mucinous tumor of the pancreas (IPMT) with invasive components are eligible.
2. Macroscopically complete resection (R0 or R1 resection).
3. Patients aged from 18 to 79 years.
4. WHO performance status 0-1.
5. No prior radiotherapy and no previous chemotherapy.
6. Full recovery from surgery and patient able to receive chemotherapy: adequate oral nutrition of ≥1500 calories per day and free of significant nausea and vomiting.
7. Adequate hematologic function (Absolute neutrophil count ANC ≥1,500 cells/mm³, platelets ≥100 000 cells/mm³ and hemoglobin ≥10 g/L - possibly after transfusion -).
8. Serum total bilirubin ≤1.5 times the institutional upper limit of normal.
9. Creatinine level \<130 micromol/L (14.7 mg/L).
10. Patient of child-bearing potential (for female patient: study entry after a menstrual period and a negative pregnancy test) must agree to use two medically acceptable methods of contraception (one for the patient and one for the partner) during the study and for 4 months after the last study treatment intake for women and 6 months for men.
11. Interval since surgery between 21 and 84 days.
12. Patient information and signed informed consent.
13. Public or private health insurance coverage.
Exclusion Criteria:
1. Other types of non-ductal tumor of the pancreas, including endocrine tumors or acinar cell adenocarcinoma, cystadenocarcinoma and malignant ampulloma.
2. Metastases (including ascites or malignant pleural effusion).
3. Macroscopic incomplete tumor removal (R2 resection).
4. CA 19-9 \> 180 U/ml within 21 days of registration on study.
5. No heart failure or coronary heart disease symptoms.
6. No major comorbidity that may preclude the delivery of treatment or active infection (HIV or chronic hepatitis B or C) or uncontrolled diabetes.
7. Pre-existing neuropathy, Gilbert's disease or genotype UGT1A1 \* 28 / \* 28.
8. Inflammatory disease of the colon or rectum, or occlusion or sub-occlusion of the intestine or severe postoperative uncontrolled diarrhea.
9. Concomitant occurrence of another cancer, or history of cancer except in situ carcinoma of the cervix treated or basal cell carcinoma or squamous cell carcinoma.
10. Fructose intolerance.
11. Persons deprived of liberty or under guardianship.
12. Psychological, familial, sociological or geographical condition potentially. hampering compliance with the study protocol and follow-up schedule.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
79 Years
Study:
NCT01526135
Study Brief:
Protocol Section:
NCT01526135