UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029773
Receipt number R000034020
Scientific Title The Impact of oral medication on cognitive function and delirium in patients with acute congestive heart failure
Date of disclosure of the study information 2017/11/01
Last modified on 2023/02/28 16:26:40

* 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 Impact of oral medication on cognitive function and delirium in patients with acute congestive heart failure

Acronym

Oral medication and cognitive function in heart failure patients

Scientific Title

The Impact of oral medication on cognitive function and delirium in patients with acute congestive heart failure

Scientific Title:Acronym

Oral medication and cognitive function in heart failure patients

Region

Japan


Condition

Condition

acute heart failure

Classification by specialty

Medicine in general Cardiology Geriatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate whether oral medication for hospitalized patients with acute heart failure decrease the occurrence of delirium and impairment of cognitive function compared with conventional intravenous infusion treatment.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

frequency of delirium

Key secondary outcomes

cognitive function


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking

YES

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

conventional intravenous treatment

Interventions/Control_2

oral treatment (avoiding continuous intravenous therapy)

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

65 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

agreement by patients
beyond 65 years old
diagnosed with acute congestive heart failure

Key exclusion criteria

acute myocardial infarction
severe respiratory failure (PaO2<60Torr, and/or SPO2<90% on oxygen administration)
shock vital (sBP<90mmHg)

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Masashi Kasao

Organization

Tokyo Metropolitan Police Hospital

Division name

Department of Cardiology

Zip code


Address

4-22-1, Nakano, Nakano, Tokyo, 164-8541

TEL

+81-3-5343-5611

Email

mu3948@hotmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Kazutaka Ueda

Organization

Tokyo Metropolitan Police Hospital

Division name

Department of Cardiology

Zip code


Address

4-22-1, Nakano, Nakano, Tokyo, 164-8541

TEL

+81-3-5343-5611

Homepage URL


Email

ueda-cib@umin.ac.jp


Sponsor or person

Institute

Tokyo Metropolitan Police Hospital

Institute

Department

Personal name



Funding Source

Organization

Tokyo Metropolitan Police Hospital

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

東京警察病院(東京都)


Other administrative information

Date of disclosure of the study information

2017 Year 11 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

Completed

Date of protocol fixation

2017 Year 09 Month 20 Day

Date of IRB

2019 Year 03 Month 13 Day

Anticipated trial start date

2019 Year 04 Month 01 Day

Last follow-up date

2021 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 10 Month 31 Day

Last modified on

2023 Year 02 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034020


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name