ClinConnect ClinConnect Logo
Search / Trial NCT03540875

Automated Anesthesia Guided by the Conox Monitor for Surgery

Launched by CMC AMBROISE PARÉ · May 17, 2018

Trial Information

Current as of May 19, 2025

Terminated

Keywords

Anesthesia, General Total Intravenous Anesthesia Closed Loop Anesthesia Conox Eeg Monitoring Q Con Q Nox

ClinConnect Summary

Several monitors are currently proposed to evaluate the depth of hypnosis. The Conox monitor differentiates itself from the other brain monitor by calculating two EEG indexes, the qCon and the qNox. The qCon corresponds to the depth of the sedation and the qNox relates to the probability that a nociceptive stimulation triggers a movement of the patient. A controller allowing the automated titration of propofol guided by the qCon and remifentanil guided by the qNox has been developed. In preparation for a large multi-center control trial, this prospective randomized study evaluates the effec...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Scheduled surgery for at least one hour
  • Consent for participation
  • Affiliation to the social security system
  • Exclusion Criteria:
  • Pregnant or breastfeeding women
  • Patients for which Conox monitor should not be used
  • Allergies to propofol or remifentanil

About Cmc Ambroise Paré

CMC Ambroise Paré is a distinguished clinical trial sponsor dedicated to advancing medical research and innovation. With a focus on enhancing patient care, the organization specializes in the development and management of clinical trials across various therapeutic areas. CMC Ambroise Paré is committed to rigorous scientific standards, ensuring compliance with regulatory requirements while fostering collaboration among healthcare professionals, researchers, and stakeholders. By leveraging cutting-edge methodologies and a patient-centric approach, the organization aims to contribute to the development of safe and effective treatments, ultimately improving health outcomes and quality of life.

Locations

Besançon, Bourgogne Franche Comté, France

Suresnes, Ile De France, France

Soyaux, Poitou Charentes, France

Patients applied

0 patients applied

Trial Officials

Marc Fischler, MD

Study Chair

Hôpital Foch

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials