Viewing Study NCT06487442



Ignite Creation Date: 2024-07-17 @ 11:58 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06487442
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-05
First Post: 2024-06-27

Brief Title: Management of Postoperative Pain in France a Prospective National Study
Sponsor: Société Française dAnesthésie et de Réanimation
Organization: Société Française dAnesthésie et de Réanimation

Study Overview

Official Title: Management of Postoperative Pain in France a Prospective National Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: ALGOSFAR2
Brief Summary: Managing postoperative pain is an ongoing challenge Therefore frequent surveys are needed to constantly evaluate and improve perioperative pain care The French reference audit was published in 2008 Ten years later the French AlgoSFAR survey of 70 centres and 3315 patients highlighted a clear improvement in practices However these data have never been published in a referenced journal due to significant methodological biases

In 2024 we do not have recent French data based on rigorous methodology in the field of postoperative pain management

The objective of this study is to reassess postoperative pain management in France This is a prospective national survey The proposed methodology will make it possible to provide a relevant snapshot of the practices and quality of care Secondarily areas for improvement can be identified and these results will also help in the drafting of future recommendations

100 centres representative of the French map of surgical centres will be contacted

Inclusions will take place over 2 days identical for all centres All patients eligible for inclusion during this period will be included
Detailed Description: None

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