UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053496
Receipt number R000061059
Scientific Title A prospective study to investigate the utility of preoperative ICU orientation for the prevention of postoperative delirium in cardiovascular surgery
Date of disclosure of the study information 2024/02/01
Last modified on 2024/01/31 16:38:42

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Basic information

Public title

A prospective study to investigate the utility of preoperative ICU orientation for the prevention of postoperative delirium in cardiovascular surgery

Acronym

A prospective study to investigate the utility of preoperative ICU orientation for the prevention of postoperative delirium in cardiovascular surgery

Scientific Title

A prospective study to investigate the utility of preoperative ICU orientation for the prevention of postoperative delirium in cardiovascular surgery

Scientific Title:Acronym

A prospective study to investigate the utility of preoperative ICU orientation for the prevention of postoperative delirium in cardiovascular surgery

Region

Japan


Condition

Condition

Cardiac disease, Aortic disease, Delirium

Classification by specialty

Cardiology Vascular surgery Psychiatry
Intensive care medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

A prospective, single-arm study to determine whether this orientation is effective in reducing the incidence of postoperative delirium in cardiovascular surgery

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The incidence of postoperative delirium in ICU

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Preoperative orientation regarding the postoperative ICU environment and delirium

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients 20 years of age or older who will be performed scheduled cardiovascular surgery at our hospital and who will be admitted to the ICU after surgery

Key exclusion criteria

Emergent surgery
Patients who aren not admitted to the ICU after surgery
Patients under 20 years old
Patients who do not accept the examination

Target sample size

80


Research contact person

Name of lead principal investigator

1st name Ryo
Middle name
Last name Nakamura

Organization

Wamayama medical university

Division name

Cardiothoracic surgery

Zip code

641-8519

Address

811-1 Kimiidera, wakayama city, Japan

TEL

073-441-0615

Email

m09077rn@wakayama-med.ac.jp


Public contact

Name of contact person

1st name Ryo
Middle name
Last name Nakamura

Organization

Wakayama medical university

Division name

Cardiothoracic surgery

Zip code

641-8509

Address

811-1 Kimiidera, wakayama city, Japan

TEL

073-441-0615

Homepage URL


Email

m09077rn@wakayama-med.ac.jp


Sponsor or person

Institute

Ryo Nakamura
Wakayama medical university, department of Cardiothoracic Surgery

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Wakayama medical university, IRB comittee

Address

811-1, Kimiidera, Wakayama city, Wakayama prefecture, Japan kimiide

Tel

073-441-0897

Email

wa-rinri@wakayama-med.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

2024 Year 02 Month 01 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

Preinitiation

Date of protocol fixation

2024 Year 01 Month 31 Day

Date of IRB


Anticipated trial start date

2024 Year 04 Month 01 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 01 Month 31 Day

Last modified on

2024 Year 01 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000061059


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name