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Pathophysiology of Inflammation After Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy

Pathophysiology of Inflammation After Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02741167
Enrollment
90
Registered
2016-04-18
Start date
2016-01-31
Completion date
2018-12-31
Last updated
2017-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peritoneal Cancer

Keywords

peritoneal surface malignancies, cytoreductive surgery, hyperthermic intraperitoneal chemotherapy

Brief summary

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.

Detailed 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.

Interventions

PROCEDURECRS and HIPEC

During CRS, all visible peritoneal tumors are removed. Consequently micrometastasis are removed with hyperthermic intraperitoneal chemotherapy

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
C reactive protein (CRP) mg/l, receiver operating characteristic (ROC)30 days

Countries

Switzerland

Contacts

Primary ContactKuno Lehmann, MD, PhD
kuno.lehmann@usz.ch+41 44 255 23 04
Backup ContactDilmurodjon Eshmuminov, MD
dilmurodjon.eshmuminov@usz.ch+41 44 255 11 11

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026