Postoperative Delirium in Patients Undergoing Cardiac Surgery
ConditionPostoperative Delirium
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorXijing Hospital
About this trial
Establish a follow-up database for postoperative delirium in cardiac surgery patients, adopt a bidirectional cohort design to simultaneously analyze the associations between "preoperative exposure factors and postoperative delirium incidence" and "postoperative delirium and long-term adverse outcomes", and clarify the predictive factors and prognostic impacts of postoperative delirium.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18 years old and above
Patients undergoing elective cardiac surgery
Disqualifiers
Organ transplantation surgery
Pregnant patients
Diagnosed with dementia or mental illness (such as schizophrenia) before surgery
Trial population
Adult patients undergoing elective cardiac surgery
Trial design
Design model
Cohort
Time perspective
Other
Treatments tested in this trial
Serum metabolic profile
Diagnostic testVenous serum samples are analyzed for serum metabolic profiles or other test
Treatment groups
1,500 Participants
are divided into 2 treatment groupsGroup A: delirium group1 intervention
Group B: control group1 intervention
Trial outcomes
Primary outcomes
1
postoperative delirium
accessed by CAM-ICU/3D-CAM
Time frame
within 1 week after operationSecondary outcomes
1
subtype of delirium
accessed by CAM-ICU/3D-CAM
Time frame
within 1 week after operation2
severity of delirium
accessed by CAM-ICU-7
Time frame
within 1 week after operation3
duration of delirium
accessed by CAM-ICU/3D-CAM
Time frame
within 1 week after operation4
PSQI score 1 morth after surgery
assessed using the Pittsburgh Sleep Quality Index
Time frame
1 morth after surgerySponsors and contacts
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Source ClinicalTrials.gov