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Pathophysiology of Inflammation After Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Unknown

Conditions

Peritoneal Cancer

Treatments

Procedure: CRS and HIPEC

Study type

Observational

Funder types

Other

Identifiers

NCT02741167
HIPEC 2015-0529

Details and patient eligibility

About

The purpose of this study is to assess the dynamics of inflammatory parameters in presence or absence of infectious complications after cytoreductive surgery with hyperthermic intraperitoneal chemotherapy.

Full description

Cytoreductive surgery with hyperthermic intraperitoneal chemotherapy is the treatment of choice in patients with primary or secondary peritoneal surface malignancies. However the survival benefit is achieved at the cost of increased morbidity and mortality due to an extensive surgery and intraoperative chemo-therapy. Among complications infectious complications are the most common. The early diagnosis of a potential fatal infection is therefore crucial to ensure a good outcome in patients.

Enrollment

90 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Consecutive adult patients (more than 18 years) subjected to CRS and HIPEC due to peritoneal malignancy.
  • Written informed consent by the participant after information about the research project

Exclusion criteria

  • No primary or secondary peritoneal surface malignancy
  • No CRS and HIPEC
  • Pregnancy
  • Younger than 18 years

Trial design

90 participants in 1 patient group

CRS and HIPEC
Description:
Patients subjected to cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) due to primary or secondary peritoneal malignancy
Treatment:
Procedure: CRS and HIPEC

Trial contacts and locations

1

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Central trial contact

Kuno Lehmann, MD, PhD; Dilmurodjon Eshmuminov, MD

Data sourced from clinicaltrials.gov

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