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Clinical Trials/NCT01617382
NCT01617382
Recruiting
N/A

Register With Data From Patients With the Diagnosis of a Peritoneal Surface Malignancy, for Which Cytoreductive Surgery and Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) is Performed

Universitaire Ziekenhuizen KU Leuven1 site in 1 country125 target enrollmentMay 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Peritoneal Carcinomatosis
Sponsor
Universitaire Ziekenhuizen KU Leuven
Enrollment
125
Locations
1
Primary Endpoint
To improve the prognosis/survival of patients with malignancies localized on the peritoneal surface.
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to register the follow-up data of patients who, because of a peritoneal surface malignancy, will undergo cytoreductive surgery and HIPEC.

Detailed Description

To register the follow-up data of patients who, because of a peritoneal surface malignancy, will undergo cytoreductive surgery and HIPEC. In this surgical intervention, the abdominal cavity is macroscopically cleared of tumor, by removing all visible tumor nodules, and is subsequently rinsed with hyperthermic (heated) chemotherapy, aiming to destroy all residual invisible tumor cells that might have stayed behind after the debulking. The eventual aim of this procedure is to improve the prognosis/survival of patients with malignancies localized on the peritoneal surface.

Registry
clinicaltrials.gov
Start Date
May 2012
End Date
December 2028
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with peritoneal carcinomatosis of colorectal origin, patients with pseudomyxoma peritonei (type DPAM or PMCA) and patients with peritoneal mesothelioma who are planned to undergo cytoreductive surgery and HIPEC because of a peritoneal surface malignancy

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

To improve the prognosis/survival of patients with malignancies localized on the peritoneal surface.

Time Frame: Follow-up over a time period of at least 5 years

Study Sites (1)

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