UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036507
Receipt number R000041560
Scientific Title Effect of sivelestat, a neutrophil elastase inhibitor on cardiac surgical patients after cardiopulmonary bypass
Date of disclosure of the study information 2019/04/14
Last modified on 2019/04/14 23:10:55

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Basic information

Public title

Effect of sivelestat, a neutrophil elastase inhibitor on cardiac surgical patients after cardiopulmonary bypass

Acronym

Effect of sivelestat, a neutrophil elastase inhibitor on cardiac surgical patients after cardiopulmonary bypass

Scientific Title

Effect of sivelestat, a neutrophil elastase inhibitor on cardiac surgical patients after cardiopulmonary bypass

Scientific Title:Acronym

Effect of sivelestat, a neutrophil elastase inhibitor on cardiac surgical patients after cardiopulmonary bypass

Region

Japan


Condition

Condition

cardiac and aortic disease

Classification by specialty

Cardiovascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the effect of sivelestat administration in cardiac surgical patients

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

perioperative cytokine in bronchial bronchiolar lavage fluid, pulmonary function, oxygenation.

Key secondary outcomes

myocardial injury, hemodynamics, perioperative cytokine in blood


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

0.9 % saline 2ml/hr for 24 hours

Interventions/Control_2

sivelestat 0.2mg/kg/hr for 24 hours

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

cardiac surgical patients undergoing cardiopulmonary bypass

Key exclusion criteria

shock, pulmonary edema, liver dysfunction

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Masahiro
Middle name
Last name Fujii

Organization

Nippon Medical School

Division name

Cardiovascular surgery

Zip code

113-8603

Address

1-1-5 Sendagi, Bunkyo, Tokyo

TEL

03-3822-2131

Email

mfujii-cvs@umin.ac.jp


Public contact

Name of contact person

1st name Masahiro
Middle name
Last name Fujii

Organization

Nippon Medical School

Division name

Cardiovascular surgery

Zip code

113-8603

Address

1-1-5 Sendagi, Bunkyo, Tokyo

TEL

03-3822-2131

Homepage URL


Email

mfujii-cvs@umin.ac.jp


Sponsor or person

Institute

Nippon Medical School

Institute

Department

Personal name



Funding Source

Organization

Nippon Medical School

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

03-3822-2131

Address

1-1-5 Sendagi, Bunkyo, Tokyo

Tel

03-3822-2131

Email

mfujii-cvs@umin.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

2019 Year 04 Month 14 Day


Related information

URL releasing protocol

DOI: 10.1510/icvts.2009.225243

Publication of results

Partially published


Result

URL related to results and publications

DOI: 10.1510/icvts.2009.225243

Number of participants that the trial has enrolled

30

Results

In the control group, the levels of PMN elastase, IL-6, IL-8 in BAL showed a increase after CPB initiation, and were maintained at high levels 3 hours after CPB. In contrast, the sivelestat group had lower concentrations of PMN elastase, IL-6, IL-8 during and after CPB.
The reduction in PaO2/FiO2 ratio after CPB was strongly related to the increase in IL-8, IL-6 or the elevation in PMN elastase.

Results date posted

2019 Year 04 Month 14 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results

2010 Year 03 Month 30 Day

Baseline Characteristics

Control
age 65
gender M 8/F 7
VHD 11
VHD+IHD 4

Sivelestat
age 68
gender M 6/F 9
VHD 9
VHD+IHD 4
Cardiac tumor 1
TAA 1

Participant flow

Main outcome:
Control  AVR 6 cases
Sivelestat AVR 6 cases

Adverse events

none

Outcome measures

PMN elastase in BAL
during CPB post CPB
control 477 666
sivelestat 78 204 *p=0.0002

IL-6 in BAL
during CPB post CPB
control 6521 8913
sivelestat 456 3549 *p=0.029

IL-8 in BAL
during CPB post CPB
control 156 124
sivelestat 120 43 *p=0.527

P/F post CPB 3h 12h
control 33 43
sivelestat 11 17 *p=0.0086

Plan to share IPD

NO

IPD sharing Plan description

NO


Progress

Recruitment status

Main results already published

Date of protocol fixation

2004 Year 01 Month 14 Day

Date of IRB

2004 Year 01 Month 28 Day

Anticipated trial start date

2004 Year 01 Month 29 Day

Last follow-up date

2005 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

2019 Year 04 Month 14 Day

Last modified on

2019 Year 04 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041560


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name