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NCT06478056Completed

Correlation of Portal and Peripheral Venous ctDNA in Pancreatic Adenocarcinoma

Source: ClinicalTrials.gov · Last updated 6 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
12 Jun 2024
Start date
28 May 2024
Primary completion date
22 Oct 2025
Lead sponsor
University Hospital, Rouen
NCT number
NCT06478056

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 28 May 2024 to the primary completion date, 22 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Other active cancer or haematological malignancy
  • Uncontrolled major infections, chronic infectious diseases, immunodeficiency syndromes
  • Premalignant hematological disorders, e.g. myelodysplastic syndrome
  • Severe hepatic impairment
  • Pregnant, parturient or breast-feeding woman (a pregnancy test will be carried out unless there is a history of hysterectomy, tubal ligation or menopause)
  • 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.

Lab values

  • 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.

Other

  • Patients not registered with social security
  • Person deprived of liberty by an administrative or judicial decision, or person placed under court protection, sub-guardianship or guardianship.
  • Treatment contraindicated for venous sampling

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital, Rouen
Coordinator of this site? Confirm its status
RouenFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.