Actively Recruiting

All Genders
NCT01617382

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

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-06-26

125

Participants Needed

1

Research Sites

865 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with peritoneal carcinomatosis of colorectal origin, pseudomyxoma peritonei (type DPAM or PMCA), or peritoneal mesothelioma
  • Planned to undergo cytoreductive surgery and hyperthermic intra-peritoneal chemotherapy (HIPEC) due to a peritoneal surface malignancy
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Clinics Gasthuisberg

Leuven, Flemish Brabant, Belgium, 3000

Actively Recruiting

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Research Team

I

Isabelle B Terrasson

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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