Clinical trial · Interventional
Adjuvant Pressurized Intraperitoneal Aerosol Chemotherapy to Prevent Colorectal Peritoneal Metastases (ProphyPIPAC)
Pilot Study of Adjuvant Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) for the Prevention of Peritoneal Metastases After Curative-intent Surgery for High-risk Colorectal Cancer.
NCT06091683CI-TRIAL-00070646ProphyPIPACunknownN/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)
The objective of this clinical trial is to demonstrate the feasibility and safety of pressurized intraperitoneal aerosol chemotherapy (PIPAC) for the prevention of peritoneal metastases after curative-intent surgery for high-risk colorectal cancer.
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 |
|---|---|---|---|
| Peritoneal Metastases From Colorectal Cancer | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Pressurized intraperitoneal aerosol chemotherapy (PIPAC) | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Adjuvant pressurized intraperitoneal aerosol chemotherapy (PIPAC)
- description
- Preliminary laparoscopic exploration of the abdominal cavity and adjuvant pressurized intraperitoneal aerosol chemotherapy (PIPAC) with oxaliplatin and concurrent intravenous infusion of 5-fluorouracil and folinic acid.
- interventionNames
- Procedure: Pressurized intraperitoneal aerosol chemotherapy (PIPAC)
Primary outcomes (2)
- measure
- Feasibility of adjuvant pressurized intraperitoneal aerosol chemotherapy (PIPAC)
- timeFrame
- 12 weeks
- description
- The adjuvant PIPAC performed in an early setting after primary surgery will be considered feasible if: * the laparoscopic procedure can be completed in 9 patients; * the postoperative stay will be three days or shorter in ≥6 patients; * the post-operative adjuvant s-CT will begin within 12 weeks of primary surgery in ≥ 9 patients.
- measure
- Safety of adjuvant pressurized intraperitoneal aerosol chemotherapy (PIPAC)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histopathological diagnosis of intestinal type, mucinous or signet ring cell adenocarcinoma of the colon (with upper limit of the tumor above peritoneal reflection); 2. curative (microscopically complete) surgery performed by laparotomy or laparoscopy; 3. presence of at least one of the following risk factors for the development of metachronous peritoneal metastases: * perforated primary tumor (any T, N0-2b, M0); * primary tumor infiltrating the visceral peritoneum (pT4a, N0-2b, M0), or directly invading adjacent organs (pT4b, N0-2b, M0); 4. age \> 18; 5. performance status 2 according to the World Health Organization score; 6. willingness to start adjuvant systemic chemotherapy and post-operative follow-up; 7. Signing of informed consent. Exclusion Criteria: 1. active sepsis; 2. cardiac function impairment (history of previous heart failure or 40% ejection fraction); 3. renal impairment (serum creatinine \>1.5 normal value or creatinine clearance 60 ml/min); 4. liver function impairment (aspartate aminotransferase, alanine aminotransferase, bilirubin \> 1.5 normal value); 5. bone marrow function impairment (leukocytes 4000 / mm3, neutrophils 1500 /mm3, platelets 80000/mm3); 6. lung function impairment (diagnosis of severe chronic obstructive pulmonary disease or 50% forced expiratory volume at one second or 40% diffusion capacity of lung for carbon monoxide adjusted for age); 7. extra-abdominal and/or hepatic metastases at the Computed Tomography scan of the chest, abdomen and pelvis with intravenous contrast; 8. severe complications (grade 3-4) after primary cancer surgery; 9. haemorrhagic diathesis or coagulopathy; 10. pregnancy or lactation in progress; 11. psychiatric or neurological conditions such as to preclude protocol procedures; 12) contraindications to laparoscopy; 13) known hypersensitivity to oxaliplatin or other platinum containing compounds and/or to any of their excipients; 14) history of previous malignancies treated in the last three years, excluding cutaneous spinocellular carcinoma and/or basocellular carcinoma; 15) prior pre-operative radio-chemotherapy..
References
Publications (0)
Data not yet available
No reference posted for this study.