Ignite Creation Date:
2024-05-06 @ 8:05 PM
Last Modification Date:
2024-10-26 @ 3:20 PM
Study NCT ID:
NCT06248684
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-02-08
First Post:
2023-10-01
Brief Title:
Prevention of Postoperative Delirium in Elderly Patients
Sponsor:
Technical University of Munich
Organization:
Technical University of Munich
Study Overview
Official Title:
Prevention of Postoperative Delirium in the Care of Elderly Patients A Monocentric Prospective Intervention Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-01
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:
PODproject
Brief Summary:
Prevention of Postoperative Delirium in the care of Elderly Patients A Monocentric Prospective Intervention Study With the Question of Whether the Incidence Length and Severity of Postoperative Delirium Can be Reduced by Implementing a Standardised Multidimensional Delirium Management Protocol
Detailed Description:
Within the framework of a six-month observation period the investigators intend to identify risk factors of the patient collective for the development of postoperative delirium For this purpose a preoperative risk assessment is performed which includes cognitive and physical performance as well as premedication and concomitant diseases Included are patients of at least 65 years of age of defined specialties Postoperatively patients who have undergone the assessment are tested for delirium once per shift until the third postoperative day and severity and duration are documented After completion of the observation period risk factors favoring the development of postoperative delirium will be identified In the subsequent intervention period patients from the age of 65 years with an additional identified risk factor will receive standardized targeted perioperative care This includes both adherence to preventive measures in accordance with guidelines and the recommendation of therapeutic measures if a delirium is diagnosed Through the standardized interprofessional and interdisciplinary application of the described approach the investigator aim to reduce the incidence duration and severity of postoperative delirium Furthermore the evaluation of the identification of the weighting of risk factors as well as the identification of risk factors by the tests performed length of hospital stay three-month mortality and daily living skills after three months In addition a baseline EEG standardized awake EEG before initiation is recorded in a subgroup to determine whether patients at risk for delirium can be identified and whether intraoperative EEG parameters support the delirium risk assessment
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