Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06644209
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-10-14
Brief Title:
Predictive Efficacy of Ratio of Median Frequency to Spectral Edge Frequency Used in the Depth of Anaesthesia Monitoring on Post-operative Cognitive Functions
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Predictive Efficacy of Ratio of Median Frequency to Spectral Edge Frequency Used in the Depth of Anaesthesia Monitoring on Post-operative Cognitive Functions
Status:
COMPLETED
Status Verified Date:
2024-10
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:
None
Brief Summary:
The primary objective of this observational study is to evaluate the effectiveness of preoperative anaesthesia depth monitoring parameters in predicting postoperative cognitive functions in non-cardiac adult patients
Participants will preoperatively perform cognitive tests such as the Nursing Delirium Screening ScaleNu-DESC and 4 As Test4AT to assess baseline cognitive performance The same tests will be repeated twice daily until the postoperative 3rd day or discharge
Participants will preoperatively perform cognitive tests such as the Nursing Delirium Screening ScaleNu-DESC and 4 As Test4AT to assess baseline cognitive performance The same tests will be repeated twice daily until the postoperative 3rd day or discharge
Detailed Description:
The primary objective of this observational study is to evaluate the effectiveness of preoperative anaesthesia depth monitoring parameters such as Bispectral IndexBIS Spectral edge frequencySEF and Median frequencyMF in predicting postoperative cognitive functions in non-cardiac adult patients
Participants will preoperatively perform cognitive tests such as the Nursing Delirium Screening ScaleNu-DESC and 4 As Test4AT to assess baseline cognitive performance Intraoperative haemodynamic and BIS parameters will be collected via manual data entry into printed forms Also a two-channel electroencephalogramEEG and BIS parametersBIS Number SEF MF will be collected digitally
The cognitive tests will be repeated twice daily until the postoperative 3rd day or discharge
Parameters such as mean intraoperative MF value and the ratio of MF over SEF will be compared against postoperative cognitive test scores
Participants will preoperatively perform cognitive tests such as the Nursing Delirium Screening ScaleNu-DESC and 4 As Test4AT to assess baseline cognitive performance Intraoperative haemodynamic and BIS parameters will be collected via manual data entry into printed forms Also a two-channel electroencephalogramEEG and BIS parametersBIS Number SEF MF will be collected digitally
The cognitive tests will be repeated twice daily until the postoperative 3rd day or discharge
Parameters such as mean intraoperative MF value and the ratio of MF over SEF will be compared against postoperative cognitive test scores
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