Ignite Creation Date:
2024-05-06 @ 8:18 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06339385
Status:
COMPLETED
Last Update Posted:
2024-04-02
First Post:
2024-03-25
Brief Title:
Management of PADIS in Emergency Intensive Care Unit
Sponsor:
Capital Medical University
Organization:
Capital Medical University
Study Overview
Official Title:
Management of Pain Agitation-sedation Delirium Immobility and Sleep Disruption in Emergency Intensive Care Unit a Multicenter Cross-sectional Survey
Status:
COMPLETED
Status Verified Date:
2024-03
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:
None
Brief Summary:
Investigate the prevalence of PADIS in EICU as well as the awareness and clinical implementation status of medical staff towards PADIS
The investigators conducted a multicenter cross-sectional survey in mainland China including a one-day point prevalence investigation and a questionnaire survey The inclusion criteria encompassed all adult patients admitted to the participating emergency department intensive care units EDICUs during the on-site screening while exclusion criteria comprised patients aged less than 18 years EDICU stays duration less than 24 hours before the screening and participation in other concurrent trials Hospital and nursing records from the 24 hours preceding enrollment were examined to document the assessment rate of pain agitation-sedation and delirium Physicians and nurses on duty 24 hours before the patients39 enrollment was invited to complete the questionnaire survey regarding the ICU profiles professional expertise assessment and treatment of PAD early mobilization and sleep improvement practices
The investigators conducted a multicenter cross-sectional survey in mainland China including a one-day point prevalence investigation and a questionnaire survey The inclusion criteria encompassed all adult patients admitted to the participating emergency department intensive care units EDICUs during the on-site screening while exclusion criteria comprised patients aged less than 18 years EDICU stays duration less than 24 hours before the screening and participation in other concurrent trials Hospital and nursing records from the 24 hours preceding enrollment were examined to document the assessment rate of pain agitation-sedation and delirium Physicians and nurses on duty 24 hours before the patients39 enrollment was invited to complete the questionnaire survey regarding the ICU profiles professional expertise assessment and treatment of PAD early mobilization and sleep improvement practices
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