Clinical trial · Interventional
Correlation of Portal and Peripheral Venous ctDNA in Pancreatic Adenocarcinoma
NCT06478056CI-TRIAL-00102738VEINOPANcompletedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to evaluate the prognostic impact of the detection of circulating tumor DNA in peripheral venous blood, portal venous blood, collected intraoperatively, as well as its detection in peritoneal fluid.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pancreatic Cancer | Malignant Pancreatic Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| pancreatectomy | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Surgery
- description
- patients operated on for pancreatic adenocarcinoma in the digestive surgery department of Rouen University Hospital
- interventionNames
- Procedure: pancreatectomy
Primary outcomes (1)
- measure
- level of ctDNA
- timeFrame
- Surgery
- description
- the level of ctDNA measured in peripheral venous and portal blood before and after mobilization of the specimen during surgery
Secondary outcomes (2)
- measure
- level of ctDNA
- timeFrame
- surgery
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥ 18 years * Patient with operable pancreatic adenocarcinoma (resectable or boderline with or without neoadjuvant therapy) with histological evidence or indirect diagnostic criteria (CA 19-9 Significant (≥ 200 U/ml), pancreatic hypodense lesion without differential diagnosis) * Biological criteria: Neutrophils \> 1,500 cmm, platelet count \> 100,000 cmm, creatinine clearance (Cockroft and Gault equation) \> 60 ml/min, hemoglobin \> 10 g/dl. * ECOG performance status 0 or 1 * Patient has read and understood the information letter and signed the non-opposition/consent form. * For an adult unable to give consent: Representative of the adult who has read and understood the information letter and signed the consent form Exclusion Criteria: * Other active cancer or haematological malignancy * Uncontrolled congestive heart failure - untreated angina pectoris; recent myocardial infarction (within the last year) - uncontrolled hypertension (SBP \> 160 mm or DBP \> 100 mm, despite optimal drug therapy), long QT. * Uncontrolled major infections, chronic infectious diseases, immunodeficiency syndromes * Premalignant hematological disorders, e.g. myelodysplastic syndrome * Severe hepatic impairment * Patients not registered with social security * Pregnant, parturient or breast-feeding woman (a pregnancy test will be carried out unless there is a history of hysterectomy, tubal ligation or menopause) * Person deprived of liberty by an administrative or judicial decision, or person placed under court protection, sub-guardianship or guardianship. * History of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol, or to prevent him/her from giving informed consent. * Treatment contraindicated for venous sampling
References
Publications (0)
Data not yet available
No reference posted for this study.