Ignite Creation Date:
2024-05-06 @ 3:02 PM
Last Modification Date:
2024-10-26 @ 1:42 PM
Study NCT ID:
NCT04508465
Status:
UNKNOWN
Last Update Posted:
2020-09-09
First Post:
2020-07-30
Brief Title:
Persistent Postoperative Pain After Major Emergency Abdominal Surgery
Sponsor:
Zealand University Hospital
Organization:
Zealand University Hospital
Study Overview
Official Title:
Persistent Postoperative Pain After Major Emergency Abdominal Surgery
Status:
UNKNOWN
Status Verified Date:
2020-09
Last Known Status:
ENROLLING_BY_INVITATION
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:
None
Brief Summary:
Perioperative pain is one of the most significant complaints and problems for patients undergoing major open surgery Pain after surgery carry an abundance of consequences such as reduced mobilization reduced nutrition intake reduced pulmonary capacity and increased risk of complications and length of hospitalization The literature does not supply much information on short- or longer-term outcomes of pain treatment for emergency surgery The investigators know that for planned surgery in general around 10-50 percentage suffer from persistent postoperative pain It is therefore important to follow-up on the longer-term outcomes after the standardized analgesic pain treatment Based on a predefined patient group called OMEGA Optimizing Major EMergency Abdominal surgery the investigators hypothesize that OMEGA patients will present a significant incidence rate of patients with persistent postoperative pain andor continued opioidnon-opioid usage Therefore this study is to investigate the incidence of prolonged postoperative pain and opioidnon-opioid consumption in OMEGA patients at 3 month after major emergency abdominal surgery
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