Viewing Study NCT06437743



Ignite Creation Date: 2024-06-16 @ 11:49 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06437743
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-31
First Post: 2024-05-25

Brief Title: Monitoring Nociception Using NoL Index to Reduce Opioid-Related Complications in Laparoscopic Abdominal Surgery
Sponsor: Investigation Group Anesthesia Resuscitation And Perioperative Medicine of Aragon
Organization: Investigation Group Anesthesia Resuscitation And Perioperative Medicine of Aragon

Study Overview

Official Title: Monitoring Nociception Using NoL Index and Its Implications in Reducing Opioid-Related Complications in Laparoscopic Abdominal Surgery
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SIMONE
Brief Summary: This study aims to determine if optimal intraoperative nociception monitoring using the NoL index can reduce postoperative complications related to opioid use in laparoscopic abdominal surgery The hypothesis is that guided nociception monitoring decreases opioid-related complications and improves postoperative outcomes
Detailed Description: The study is a prospective observational cohort study conducted across multiple centers It aims to evaluate the impact of intraoperative nociception monitoring on postoperative opioid-related complications The study will involve two groups of patients undergoing laparoscopic abdominal surgery one group with visible NoL monitoring and another with non-visible NoL monitoring

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None