Fact CheckerSign in

NCT06929013Recruiting

Blood Clearance Kinetics of the Nucleosome and CTCF in Peritoneal Metastasis Colorectal Cancer.

Monitoring of Blood Clearance Kinetics of the Nucleosome and CTCF in Peri-operative Management of Peritoneal Metastasis Colorectal Cancer.

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

Colorectal cancer is highly prevalent in France, ranking second among women and third among men. Its primary metastatic sites include the liver, lungs, and peritoneum. For peritoneal metastases, when the disease is moderately extensive, cytoreductive surgery is recommended in an expert centre. Following this procedure, the surgeon uses the CC-Score (Completeness of Cytoreduction after Surgery Score) to assess the completeness of surgical resection by evaluating the largest remaining tumor residue. This subjective score is currently the main prognostic factor for oncological outcomes post-surgery. However, there is no objective score based on biological criteria to evaluate the radicality of resection, despite the hypothesis that the micrometastatic component of the disease could be biologically assessed using appropriate circulating markers. New biomarkers are emerging and appear relevant for determining the presence of tumor residual disease. Notable among these are circulating tumor DNA, which can detect mutated DNA released by tumor cells into the patient's blood through high-throughput sequencing, and new markers related to epigenetic modifications in cancer cells. These markers target specific nucleosomes or the transcription factor CTCF and show promise in detecting residual disease. To effectively use these markers for constructing a biological score to detect residual disease in peritoneal carcinomatosis, it is essential to understand their perioperative kinetics. This is crucial because cellular debris release is expected post-surgery, necessitating the determination of the most relevant time point for measurement. Additionally, these markers appear to be correlated with blood inflammation levels, requiring a description of this correlation to account for this potential confounding factor. Finally, the sensitivity and specificity of these markers must be determined by studying their perioperative kinetics in patient groups undergoing surgeries other than cytoreductions for peritoneal carcinomatosis.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
58 (estimated)
First submitted
25 Mar 2025
Start date
6 May 2025
Primary completion date
20 Jun 2026
Lead sponsor
Hospices Civils de Lyon
NCT number
NCT06929013

What you commit to

  • Study type: Interventional
  • Planned participants: 58
  • From 6 May 2025 to the primary completion date, 20 Jun 2026
  • 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.

Who the study is looking for

  • Common criteria:
    • Male/female over 18 years of age.
    • Weight ≥ 55 kg at inclusion.
    • Signature of a free and informed consent form.
  • Specific criteria:
    • Group 1:
  • Peritoneal metastases colorectal cancer histologically proven
  • Synchronous or metachronous peritoneal metastases.
  • Patients eligible for initial cytoreduction surgery.
  • Non mucinous tumor (mucinous cells contingent \<30%).
    • Group 2:
    • Colorectal cancer
    • Group 3:
    • Non-oncological chronic inflammatory diseases
    • Group 4:
    • Non-oncological chronic inflammatory diseases : parietal repairs, elective sigmoidectomy for diverticulosis
    • Group 5:
    • Abdominal sepsis conditions: peritonitis due to digestive perforation in non-oncological pathology, non-perforated appendicitis, cholecystitis.
    • Non inclusion Criteria:
  • Patient with an active cancer (excluding colorectal cancer).
  • Person with a progressive autoimmune disease.

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
Hopital Lyon Sud
Coordinator of this site? Confirm its status
Pierre-BéniteFranceRecruiting

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