UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056838
Receipt number R000064593
Scientific Title Predictors of Postoperative Delirium in Cardiovascular Surgery Patients
Date of disclosure of the study information 2025/01/31
Last modified on 2025/01/27 18:04:02

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Basic information

Public title

Relationship between preoperative higher brain function and postoperative delirium in cardiovascular surgery patients

Acronym

Postoperative delirium in cardiovascular surgery patients

Scientific Title

Predictors of Postoperative Delirium in Cardiovascular Surgery Patients

Scientific Title:Acronym

Relationship between preoperative higher brain function and postoperative delirium in cardiovascular surgery patients.

Region

Japan


Condition

Condition

Patients undergoing cardiovascular surgery

Classification by specialty

Cardiovascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Determining the association between postoperative delirium and preoperative cognitive function in patients undergoing cardiovascular surgery.

Basic objectives2

Others

Basic objectives -Others

Analysis of perioperative factors

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Occurrence of delirium

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

100 years-old >

Gender

Male and Female

Key inclusion criteria

Patients undergoing cardiovascular surgery

Key exclusion criteria

Patients with postoperative cerebrovascular complications
Patients with difficulty in preoperative assessment of MMSE FAB IQ
Patients with procedures other than open heart surgery
Patients with missing values
Patients who have requested not to participate in the study via a published opt-out document

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Tomohiro
Middle name
Last name Nakajima

Organization

Sapporo Medical University

Division name

Cardiovascular surgery

Zip code

0608543

Address

Sapporo City South 1 West 16

TEL

011-611-2111

Email

t.nakajima@sapmed.ac.jp


Public contact

Name of contact person

1st name Tomohiro
Middle name
Last name Nakajima

Organization

Sapporo Medical University

Division name

Cardiovascular surgery

Zip code

0608543

Address

Sapporo City South 1 West 16

TEL

011-611-2111

Homepage URL


Email

t.nakajima@sapmed.ac.jp


Sponsor or person

Institute

Sapporo Medical University

Institute

Department

Personal name



Funding Source

Organization

Sapporo Medical University

Organization

Division

Category of Funding Organization

Local Government

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Sapporo Medical University

Address

Sapporo City South 1 West 16

Tel

011-611-2111

Email

t.nakajima@sapmed.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2025 Year 01 Month 31 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Open public recruiting

Date of protocol fixation

2024 Year 07 Month 29 Day

Date of IRB

2024 Year 07 Month 29 Day

Anticipated trial start date

2024 Year 07 Month 29 Day

Last follow-up date

2025 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2025 Year 01 Month 27 Day

Last modified on

2025 Year 01 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064593