Bioimpedance Measurement of Abdominal Free Flaps During Arterial and Venous Weaning in Breast Reconstruction

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCentre Hospitalier Universitaire, Amiens

About this trial

As the occurrence of thrombosis in post surgery is rare, it seemed difficult to study only this one. This is why we decided to test the bioimpedance, temperature and green, red and infrared light absorption measurements of the prototype during the weaning of the flap during surgery. Indeed, during weaning the investigators voluntarily interrupt the arterial and venous flow to transfer the flap to the breast. This weaning corresponds to a thrombosis model.

The patients will benefit from an "improved" postoperative monitoring. Indeed, in addition to the classical clinical monitoring, they will benefit from an additional monitoring during 5 days thanks to the realization of an ultrasound of the flap which will be carried out every 6 hours the first 24 hours then every 12 hours.

This protocol is therefore a feasibility study for the collection of data of interest.

Eligibility criteria

Qualifiers

Woman undergoing microsurgical breast reconstruction using a free abdominal flap

Age greater than or equal to 18 years

Disqualifiers

Pregnant patient

Patient with an active implantable device such as a pacemaker or an artificial heart

Patient refusing to participate in the study

Age less than 18 years old

Trial design

Treatments tested in this trial

  • portable prototype of bioimpedance measurement

Treatment groups

No treatment groups listed