UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000048102
Receipt number R000054824
Scientific Title Pharmacokinetics of milrinone with congestive heart failure
Date of disclosure of the study information 2022/06/20
Last modified on 2023/04/16 13:28:30

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Basic information

Public title

Pharmacokinetics of milrinone with congestive heart failure

Acronym

Pharmacokinetics of milrinone with congestive heart failure

Scientific Title

Pharmacokinetics of milrinone with congestive heart failure

Scientific Title:Acronym

Pharmacokinetics of milrinone with congestive heart failure

Region

Japan


Condition

Condition

cardiac

Classification by specialty

Cardiovascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To measure renal function and blood levels in patients taking milrinone to clarify the relationship between treatment effects and adverse reactions.

Basic objectives2

Pharmacokinetics

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Volume of distribution, clearance and lowest blood concentration

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

99 years-old >

Gender

Male and Female

Key inclusion criteria

Patients using milrinone after cardiopulmonary bypass during cardiovascular surgery

Key exclusion criteria

Patients more than 20% circadian variation in renal function over 12 hours

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Takahiro
Middle name
Last name Tamura

Organization

Nagoya Univeristy

Division name

Anesthesiology

Zip code

466-8550

Address

Showa-ku

TEL

0527412111

Email

takahiro@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name Takahiro
Middle name
Last name Tamura

Organization

Nagoya University Graduate School of Medicine

Division name

Anesthesiology

Zip code

466-8550

Address

Nagoya

TEL

0527412111

Homepage URL


Email

takahiro@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Nagoya University Graduate School of Medicine

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nagoya University Graduate School of Medicine

Address

Tsurumai-cho 65, Showa-ku

Tel

0527412111

Email

takahiro@med.nagoya-u.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

2022 Year 06 Month 20 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

Enrolling by invitation

Date of protocol fixation

2021 Year 08 Month 01 Day

Date of IRB

2022 Year 09 Month 03 Day

Anticipated trial start date

2021 Year 09 Month 03 Day

Last follow-up date

2022 Year 12 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

2022 Year 06 Month 20 Day

Last modified on

2023 Year 04 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000054824


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name