Intraoperative Neuromonitoring of Pelvic Autonomous Nerve Plexus During Total Mesorectal Excision

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorLarissa University Hospital

About this trial

The purpose of this research protocol is the evaluation of the improvement of the anorectal and urogenital urinary function, alongside the postoperative quality of life after the application of pIONM in patients submitted to TME for rectal cancer.

Eligibility criteria

Qualifiers

Histologically confirmed rectal cancer

Surgical resection with TME

<90 years old

Signed informed consent

Disqualifiers

Emergency operation

Presence of pacemaker

Partial mesorectal excision

Sepsis or systematic infection

Trial design

Treatments tested in this trial

  • Pelvic Intraoperative Neuromonitoring

Treatment groups

44 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Larissa University Hospital

Lead sponsor

General Hospital of Larissa

Collaborator

University of Thessaly

Collaborator