Viewing Study NCT06555107



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06555107
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-13

Brief Title: Acute Preoperative Pain and Chronic Post-surgical Pain in Emergency Surgery
Sponsor: None
Organization: None

Study Overview

Official Title: Acute Preoperative Pain and Chronic Post-surgical Pain in Emergency Surgery
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: POCSE
Brief Summary: Studies evaluating postoperative pain as a risk factor for CPSP are almost exclusively carried out in the context of scheduled surgery As a result the preoperative pain studied as a risk factor for chronicity is essentially a state of pain that has persisted for several weeks or even several months

In emergency surgeries patients are subject to acute preoperative pain of varying intensity and the duration of which may vary by a few days A few studies have highlighted the intensity of acute preoperative pain as a factor favouring moderate to severe postoperative pain At this point no study has addressed the long-term consequences of this intense preoperative pain the emergency context

An evaluation in the field of emergency surgery where the preoperative pain is often intense and limited in time would enable us to identify more precisely the impact of acute pain on the incidence of CPSP

The investigators are hypothesising that the occurrence of CPSP at 3 months in patients undergoing emergency orthopaedic or abdominal surgery is associated with acute preoperative pain
Detailed Description: None

Study Oversight

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