UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000042104
Receipt number R000048051
Scientific Title Study on the relationship between postoperative delirium and blood ascorbic acid levels in patients undergoing cardiovascular surgery
Date of disclosure of the study information 2020/10/13
Last modified on 2023/07/14 00:30:08

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Basic information

Public title

Study on the relationship between postoperative delirium and blood ascorbic acid levels in patients undergoing cardiovascular surgery

Acronym

Study on the relationship between postoperative delirium and blood ascorbic acid levels in patients undergoing cardiovascular surgery

Scientific Title

Study on the relationship between postoperative delirium and blood ascorbic acid levels in patients undergoing cardiovascular surgery

Scientific Title:Acronym

Study on the relationship between postoperative delirium and blood ascorbic acid levels in patients undergoing cardiovascular surgery

Region

Japan


Condition

Condition

postoperative delirium

Classification by specialty

Cardiovascular surgery Intensive care medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine whether preoperative and postoperative ascorbic acid blood levels are associated with the development of postoperative delirium in patients undergoing cardiovascular surgery using cardiopulmonary bypass.

Basic objectives2

Others

Basic objectives -Others

To examine whether preoperative and postoperative ascorbic acid blood levels are associated with the development of postoperative delirium in patients undergoing cardiovascular surgery using cardiopulmonary bypass.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

development of postoperative 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

70 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

elective cardiovascular surgery using cardiopulmonary bypass

Key exclusion criteria

dementia

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Yusuke
Middle name
Last name Iizuka

Organization

Saitama medical center, jichi university

Division name

department of critical care and anesthesiology

Zip code

3308503

Address

1-847 Amanuma town, Omiya Ku, Saitama City, Saitama

TEL

0486472111

Email

yiizuka@jichi.ac.jp


Public contact

Name of contact person

1st name Yusuke
Middle name
Last name Iizuka

Organization

Saitama medical center, jichi university

Division name

department of critical care and anesthesiology

Zip code

3308503

Address

1-847 Amanuma town, Omiya Ku, Saitama City, Saitama

TEL

0486472111

Homepage URL


Email

yiizuka@jichi.ac.jp


Sponsor or person

Institute

jichi university

Institute

Department

Personal name



Funding Source

Organization

KAKENHI

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

Saitama medical center, jichi university

Address

1-847 Amanuma town, Omiya Ku, Saitama City, Saitama

Tel

0486472111

Email

yiizuka@jichi.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

2020 Year 10 Month 13 Day


Related information

URL releasing protocol

https://www.mdpi.com/2308-3425/10/7/293

Publication of results

Published


Result

URL related to results and publications

https://www.mdpi.com/2308-3425/10/7/293

Number of participants that the trial has enrolled

100

Results

We enrolled 100 patients, and the data of 98 patients were analyzed. Results: In total, 31 patients developed delirium, while 67 did not. Preoperative plasma ascorbic acid levels did not differ between the non-delirium and delirium groups. Postoperative plasma ascorbic acid levels were significantly different between the groups. Conclusion: In patients who undergo cardiovascular surgery with CPB, lower postoperative plasma ascorbic acid levels may be associated with the development of delirium.

Results date posted

2023 Year 07 Month 14 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

Patients older than 70 years of age scheduled for elective cardiovascular surgery using cardiopulmonary bypass.

Participant flow

Written informed consent was obtained from all patients.

Adverse events

none

Outcome measures

The incidence of postoperative delirium.

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2020 Year 07 Month 15 Day

Date of IRB

2020 Year 07 Month 15 Day

Anticipated trial start date

2020 Year 09 Month 01 Day

Last follow-up date

2021 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

To investigate the association between blood ascorbic acid levels and the development of delirium before and 24 hours after surgery.


Management information

Registered date

2020 Year 10 Month 13 Day

Last modified on

2023 Year 07 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048051


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name