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Search / Trial NCT04949646

Intraoperative Neuromonitoring of Pelvic Autonomous Nerve Plexus During Total Mesorectal Excision

Launched by LARISSA UNIVERSITY HOSPITAL · Jun 30, 2021

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

Intraoperative Neuromonitoring Pelvic Autonomous Total Mesorectal Excision

ClinConnect Summary

This clinical trial is investigating a technique called intraoperative neuromonitoring (pIONM) during a specific surgery known as Total Mesorectal Excision (TME) for patients with rectal cancer. The main goal of the study is to see if using this method can help improve bowel and urinary function after surgery, as well as enhance the overall quality of life for patients recovering from this procedure.

To participate in the trial, individuals should be between the ages of 18 and 90 and must have a confirmed diagnosis of rectal cancer that requires surgical removal through TME. Participants need to be able to provide consent and should not have certain medical conditions, such as infections or the presence of a pacemaker. Those who join the study can expect close monitoring during and after their surgery, with a focus on how well their bowel and urinary functions recover. This trial is currently recruiting participants, and by taking part, individuals can contribute to valuable research that may improve future treatments for rectal cancer.

Gender

ALL

Eligibility criteria

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

About Larissa University Hospital

Larissa University Hospital is a leading academic medical institution dedicated to advancing healthcare through innovative clinical research and education. As a prominent sponsor of clinical trials, the hospital integrates cutting-edge scientific inquiry with patient-centered care, fostering a collaborative environment for researchers, healthcare professionals, and participants. With a commitment to improving medical outcomes, Larissa University Hospital emphasizes ethical practices, rigorous methodologies, and interdisciplinary approaches in its clinical trials, contributing significantly to the development of new therapies and interventions across various medical fields.

Locations

Larissa, , Greece

Patients applied

0 patients applied

Trial Officials

Konstantinos Tepetes, Prof

Study Director

Department of Surgery, University Hospital of Larissa

Konstantinos Perivoliotis, MD

Principal Investigator

Department of Surgery, University Hospital of Larissa

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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