RecruitingNot ApplicableNCT04949646

Intraoperative Neuromonitoring of Pelvic Autonomous Nerve Plexus During Total Mesorectal Excision


Sponsor

Larissa University Hospital

Enrollment

44 participants

Start Date

Sep 19, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 18 YearsMax Age: 90 Years

Inclusion Criteria4

  • Histologically confirmed rectal cancer
  • Surgical resection with TME
  • \<90 years old
  • Signed informed consent

Exclusion Criteria8

  • Emergency operation
  • Presence of pacemaker
  • Partial mesorectal excision
  • Sepsis or systematic infection
  • Physical or mental impairment
  • Pregnancy or nursing
  • Insufficient preoperative data for the urogenital/ anorectal function
  • Lack of compliance with the research process

Interventions

OTHERPelvic Intraoperative Neuromonitoring

Pelvic Intraoperative Neuromonitoring (pIONM) allows mapping of the pelvic autonomous plexus during total mesorectal excision (TME).


Locations(1)

University Hospital of Larissa

Larissa, Greece

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04949646


Related Trials