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Peritoneal CarcinomatosisHIPECNCT01617382

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

An observational study of Peritoneal Carcinomatosis and Pseudomyxoma Peritonei, run by Universitaire Ziekenhuizen KU Leuven at 1 site in Belgium.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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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. Read more about this study

Who is it for?
Any age
How many people
125 participants
Where
1 siteBelgium
Study dates
May 2012to Dec 2028
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: 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.

Who may be able to join

  • 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

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Belgium1 site, 1 recruiting
  • University Clinics Gasthuisberg

    Leuven, Flemish Brabant, 3000

    Isabelle B Terrasson, +32 16 340837, isabelle.terrasson@uzleuven.be

    Daphne Hompes, MD, +32 16 341826, daphne.hompes@uzleuven.be

    Recruiting

Other trials in Belgium

About this study

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

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.

Read the 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.

Keywords
HIPEC, Hyperthermic (heated) chemotherapy after debulking
Medical subject headings
Peritoneal Neoplasms, Pseudomyxoma Peritonei, Fever

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01617382
Study groupRoleWhat they receive
RegistryPatients 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

What is being measured

The primary outcome is the main question the study is designed to answer.

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

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Jun 2012 (estimated)
  2. Study startMay 2012
  3. Primary completionDec 2028 (estimated)
  4. Study completionDec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
125 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01617382
Sponsor's protocol ID
S-54350
Acronym
HIPEC
Status last verified
Sep 2026
First submitted
8 Jun 2012
Last updated
3 Sep 2026
Results posted
No
Data monitoring committee
No
Individual data sharing
No

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