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NCT01617382 Clinical Trial

Register With Patients in Which Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) Was Performed

Peritoneal Carcinomatosis Clinical Trial

— HIPEC  

Official title:
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

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01617382
Other study ID # S-54350
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 2012
Est. completion date December 2026

Study information
Verified date March 2023
Source Universitaire Ziekenhuizen KU Leuven
Contact Isabelle B Terrasson
Phone +32 16 340837
Email isabelle.terrasson@uzleuven.be
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 125
Est. completion date December 2026
Est. primary completion date December 2026
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Belgium University Clinics Gasthuisberg Leuven Flemish Brabant

Sponsors (1)
Lead Sponsor Collaborator
Universitaire Ziekenhuizen KU Leuven

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary To improve the prognosis/survival of patients with malignancies localized on the peritoneal surface. Follow-up over a time period of at least 5 years
See also
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