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CompletedNCT02862899CHIPOFILUpdated Feb 9, 2026

Use of a Heating Cable to Obtain Hyperthermia During Intraperitoneal Chemotherapy

An interventional study of Thermowire in Intraperitoneal Chemotherapy, sponsored by Centre Hospitalier Universitaire Dijon. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-09.

Sponsored by Centre Hospitalier Universitaire Dijon · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
13
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The investigator will study the possibility of in situ heating of the liquid containing the chemotherapy, so as to avoid the need for an external pumping system with its complexity, and its associated risks and costs.

The use of a heating cable (prototype hereinafter called Thermowire, made by the company EFS, which is in charge of its development) was patented and tested in pigs in two studies that included 15 animals altogether (in 7 of which the heating cable was used). The aim of the first study was the purely safety aspects, while the efficacy to obtain hyperthermia, the quality and the homogeneity of the hyperthermia and its effect on the tissue penetration of the chemotherapy were evaluated in a second study. The results obtained justify transfer to use in humans in the context of a clinical trial so as to obtain CE certification.

02

Conditions studied

  • Intraperitoneal Chemotherapy
03

In context

Lead sponsor

Centre Hospitalier Universitaire Dijon is the lead sponsor of 495 studies on the registry; 105 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with national health insurance cover
  • With scheduled hyperthermic intraperitoneal chemotherapy (HIPEC) because of known peritoneal disease (primary or secondary)
  • Who have provided written consent

Exclusion criteria

Exclusion Criteria:

  • Persons under guardianship
  • Persons under 18 years old
  • Pregnant or breast-feeding women
  • Allergy to latex
  • Abandon of HIPEC following surgical exploration
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
13 participants (actual)

Study arms

  • Experimental
    Heating cable

    Device: Thermowire

Interventions

  • DeviceThermowire

    Also known as: Heating cable

06

What researchers measure

Primary outcomes

  1. SAE due to use of Thermowire

    In particular visceral thermal lesions or electric accidents.

    Time frame: Through study completion up to 22 months

07

Study locations

1 site
  • CHU Dijon Bourgogne
    Dijon, 21079, France
08

References and documents

Publications

  • Ortega-Deballon P, Facy O, Binquet C, Delroeux D, Rat P. CHIPOFIL: A pilot study assessing the feasibility of HIPEC without extracorporeal circuit. Pleura Peritoneum. 2019 Jul 26;4(3):20190008. doi: 10.1515/pp-2019-0008. eCollection 2019 Sep 1. PubMed 31667330 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02862899
Lead sponsor
Centre Hospitalier Universitaire Dijon
Responsible party
Sponsor
First posted
Aug 11, 2016
Start date
Jan 2015
Primary completion
Jun 2016
Completion
Jun 2016
Last update
Feb 9, 2026
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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