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Prevention of Postoperative Delirium in Elderly Patients

Prevention of Postoperative Delirium in the Care of Elderly Patients. A Monocentric, Prospective Intervention Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06248684
Acronym
PODproject
Enrollment
15000
Registered
2024-02-08
Start date
2024-02-06
Completion date
2026-12-31
Last updated
2024-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Delirium

Keywords

delirium, prevention and control, post operative delirium, delirium, risk factors, delirium, risk assessment, Baseline-EEG, cognitive tests, EEG, intraoperative

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.

Interventions

OTHERstandardized prevention and therapy measures

Patients from the age of 65 years with an additional risk factor for postoperative delirium are assigned to a multidimensional standardized perioperative care protocol.

Sponsors

Technical University of Munich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \>= 65 Years * intervention in one of the following departments: general and visceral surgery, urology, vascular surgery, orthopedics, trauma surgery, * Written consent by patient or legal guardian

Exclusion criteria

* Foreign language patients without interpreter * non-consenting patients without a legal representative

Design outcomes

Primary

MeasureTime frameDescription
Incidence of postoperative deliriumfor three days postoperatively and if the patient is delirium positive on the last day for the period until he is delirium negative or discharged from inpatient care, up to the day 90 visit at the latestPatients are examined once per shift for the described duration postoperatively using validated tests for delirium (CAM-ICU or 3D-CAM). Delirium testing is supplemented by pain assessment using the numerical rating scale (NRS).

Secondary

MeasureTime frameDescription
Severity of the postoperative deliriumfor three days postoperatively and if the patient has delirium on the last day for the period until he is delirium negative or discharged from inpatient care, up to the day 90 visit at the latestPatients are examined once per shift for the described duration postoperatively using validated tests for delirium severity (CAM-ICU or 3D-CAM). Delirium testing is supplemented by pain assessment using the numerical rating scale (NRS).
Which parameters and tests detect patients at risk for postoperative delirium?From the time of premedication until three days postoperativelyanalysis of the preoperative risk assessment, perioperative clinical parameters and postoperative delirium screening.
Can baseline and intraoperative EEG parameters be used to identify patients at risk? Does intraoperative burst suppression EEG represent a risk factor for delirium?From the patient's arrival in the operating room to three days postoperativelyAnalysis of EEG data recorded immediately before induction of anesthesia and during surgery.
duration of postoperative deliriumfor three days postoperatively and if the patient has delirium on the last day for the period until he is delirium negative or discharged from inpatient care, up to the day 90 visit at the latestPatients are examined once per shift for the described duration postoperatively using validated tests for delirium (CAM-ICU or 3D-CAM). Delirium testing is supplemented by pain assessment using the numerical rating scale (NRS).
The implementation of a delirium management protocol during the intervention period serves to improve the three-month outcome of patients at risk in terms of maintaining their autonomy or daily living skills.One-time interview three months postoperativelyPatients are asked about their daily living skills by telephone three months after their surgical procedure.
Implementation of a delirium management protocol reduces the length of hospital stay of risk patientsfrom the date of hospitalisation to the date of discharge from hospital, up to the day 90 visit at the latestThe length of inpatient stay of patients before and after implementation of standardized care is evaluated
Implementation of a delirium management protocol reduces three-month mortality in high-risk patientsQuery of the patients' death data three months postoperativelyThree-month mortality of patients before and after implementation of standardized care is evaluated
When is the diagnosis of postoperative delirium most commonly made?for three days postoperativePatients are examined once per shift for the described duration postoperatively using validated tests for delirium (CAM-ICU or 3D-CAM). Delirium testing is supplemented by pain assessment using the numerical rating scale (NRS).

Contacts

Primary ContactGerhard Prof. Dr. med. Schneider, MD
AINS@mri.tum.de+49-89-41404291
Backup ContactStefanie PD Dr. med. Pilge, MD
AINS@mri.tum.de+49-89-41404291

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026