UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000047693
Receipt number R000045410
Scientific Title The effect of postoperative delirium on a cardiopulmonary exercise testing at dischage in aged patinets undergoing cardiac surgery
Date of disclosure of the study information 2022/05/09
Last modified on 2022/11/11 23:04:42

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

The effect of postoperative delirium on a cardiopulmonary exercise testing at dischage in aged patinets undergoing cardiac surgery

Acronym

The effect of postoperative delirium on a cardiopulmonary exercise testing

Scientific Title

The effect of postoperative delirium on a cardiopulmonary exercise testing at dischage in aged patinets undergoing cardiac surgery

Scientific Title:Acronym

The effect of postoperative delirium on a cardiopulmonary exercise testing

Region

Japan


Condition

Condition

Aged patients undergoing cardiac surgery

Classification by specialty

Intensive care medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The effect of delirium on cardiopulmonary exercise testing at discharge

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

AT-VO2 VE/VCO2 slope

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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

100 years-old >

Gender

Male and Female

Key inclusion criteria

cardiac surgical patients

Key exclusion criteria

patients who did not dischage

Target sample size

70


Research contact person

Name of lead principal investigator

1st name Yuta
Middle name
Last name Shimomoto

Organization

Sakurabashi-Watanabe Hospital

Division name

Rehabilitation

Zip code

530-0001

Address

2-4-32 Umeda Kita-ku, Osaka , Japan

TEL

06-6341-8651

Email

fa-7y.28_5a.15@outlook.jp


Public contact

Name of contact person

1st name Yuta
Middle name
Last name Shimomoto

Organization

Sakurabashi-Watanabe Hospital

Division name

Rehabilitation

Zip code

530-0001

Address

2-4-32 Umeda Kita-ku Osaka, Japan

TEL

06-6341-8651

Homepage URL


Email

fa-7y.28_5a.15@outlook.jp


Sponsor or person

Institute

Sakurabashi-Watanabe Hospital

Institute

Department

Personal name



Funding Source

Organization

Sakurabashi-Watanabe Hospital

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

Sakurabashi-Watanabe Hospital IRB

Address

2-4-32 Umeda Kita-ku Osaka, Japan

Tel

06-6341-8651

Email

i_oka@watanabe-hsp.or.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

2022 Year 05 Month 09 Day


Related information

URL releasing protocol

http://www.watanabe-hsp.or.jp/hospitalinfo/optout

Publication of results

Unpublished


Result

URL related to results and publications

https://www.meeting-schedule.com/jsicm47/author.html

Number of participants that the trial has enrolled

70

Results

AT-VO2 and the slope of VCO2 and VE in the presence and absence of delirium and both values were comparable between the groups.

Results date posted

2022 Year 05 Month 09 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

Seventy patients aged 70 or older undergoing cardiac valve surgery, entered our ICU and were discharged from our hospital between June 2016 and July 2018.

Participant flow

All patients received active exercise from our rehabilitation team since the first postoperative day while on mechanical ventilation, and performed a CPX on a cycle ergometer before discharge.

Adverse events

No problem

Outcome measures

AT-VO2 VE/VCO2slope

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

No longer recruiting

Date of protocol fixation

2016 Year 06 Month 01 Day

Date of IRB

2019 Year 08 Month 01 Day

Anticipated trial start date

2016 Year 06 Month 01 Day

Last follow-up date

2020 Year 03 Month 01 Day

Date of closure to data entry

2022 Year 11 Month 01 Day

Date trial data considered complete

2022 Year 11 Month 01 Day

Date analysis concluded

2022 Year 11 Month 01 Day


Other

Other related information

None


Management information

Registered date

2022 Year 05 Month 09 Day

Last modified on

2022 Year 11 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000045410


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name