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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04734691
Other study ID # OPAC study
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date October 2021
Est. completion date November 2024

Study information

Verified date January 2021
Source University Hospital, Geneva
Contact Marwan-Julien Sleiman
Phone 0041795533197
Email marwan.sleiman@hcuge.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Colorectal cancer is the third most common cancer in men and second in women. It represent 345'346 new cases per year in Europe and 134'349 in the United States of America. The peritoneal cavity is the second most frequent site, after liver, for colorectal cancer relapse.Peritoneal carcinomatosis (PC) is found in approximately 5 % of patients diagnosed with colorectal cancer and 24% of patients with synchronous metastasis at the time of diagnosis. Eight percent of colorectal cancer patient will develop PC during the course of their disease . Currently systemic chemotherapy is the standard of care for the treatment of unresectable peritoneal carcinomatosis from colorectal cancer with a median survival rate of 16.3 months Peritoneal carcinomatosis has a poor response to systemic chemotherapy due to a weak penetration of agents into the peritoneum. A new approach of intraperitoneal carcinomatosis is now developed: Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is used to deliver intraperitoneal chemotherapy. It enhances the effect of chemotherapy because of the physical properties of aerosol and pressure. PIPAC is a safe with a 23% morbidity and tolerated technic that is now well described. We want to conduct a study to prove or infirm the superiority of PIPAC associated with systemic chemotherapy compare to systemic chemotherapy alone in peritoneal carcinomatosis from colorectal cancer


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date November 2024
Est. primary completion date October 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Patients 18 < age = 75 years old with Performance status (WHO) = 2 Histologically evidenced synchronous or metachronous PM of a colorectal cancer with a PCI = 15 (No complete resectable PC) Histologically evidenced synchronous or metachronous PM of a colorectal cancer with a PCI < 15 + liver or pulmonary unresectable metastases PCI < 15 but with progression at the restaging after the first line of chemotherapy Unresectable peritoneal relapse secondary to cytoreduction surgery Exclusion Criteria: - Patients with clinically significant ascites (> 3000 cc) - Pleural effusion requiring evacuation for respiratory failure - Small bowel occlusion with no possible food intake - Presence of comorbidities, notably serious chronic diseases or organ failure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
PIPAC
PIPAC is a laparoscopic procedure for intraperitoneal administration of chemotherapy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sleiman Marwan-Julien

Outcome

Type Measure Description Time frame Safety issue
Primary Progression free survival any clinical sign and/or morphological sign of peritoneal recurrence or death 8 months
Secondary Quality of life C30 8 months
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