UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000033726
Receipt number R000038459
Scientific Title Prospective observational study to assess perioperative cardiovascular events in patients undergoing non-cardiac surgery with prior history of percutaneous coronary intervention
Date of disclosure of the study information 2018/08/15
Last modified on 2020/02/12 22:50:14

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Basic information

Public title

Prospective observational study to assess perioperative cardiovascular events in patients undergoing non-cardiac surgery with prior history of percutaneous coronary intervention

Acronym

Observational study for perioperative cardiovascular events in patients with patients with prior history of percutaneous coronary intervention

Scientific Title

Prospective observational study to assess perioperative cardiovascular events in patients undergoing non-cardiac surgery with prior history of percutaneous coronary intervention

Scientific Title:Acronym

Observational study for perioperative cardiovascular events in patients with patients with prior history of percutaneous coronary intervention

Region

Japan


Condition

Condition

Coronary artery disease

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study is aimed to evaluate the perioperative risk of cardiovascular events and the efficacy of managements of antiplatelet therapy during non-cardiac surgery in patients with prior history of percutaneous coronary intervention.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Perioperative cardiovascular events, cardiac death, myocardial infarction, and coronary revascularization, at 30 day after the surgery

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with prior history of percutaneous coronary intervention who need to undergo non-cardiac surgery or procedure

Key exclusion criteria

Patients who undergo cardiac surgery
Patients who physicians determined are inappropriate

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Kengo
Middle name
Last name Tanabe

Organization

Mitsui Memorial Hospital

Division name

Division of cardiology

Zip code

1018643

Address

Kandaizumicho 1, Chiyoda-ku, Tokyo, Japan

TEL

03-3862-9111

Email

kengo-t@zd5.so-net.ne.jp


Public contact

Name of contact person

1st name Tetsu
Middle name
Last name Tanaka

Organization

Mitsui Memorial Hospital

Division name

Division of cardiology

Zip code

1018643

Address

Kandaizumicho 1, Chiyoda-ku, Tokyo, Japan

TEL

03-3862-9111

Homepage URL


Email

ttanaka@mitsuihosp.or.jp


Sponsor or person

Institute

Mitsui Memorial Hospital

Institute

Department

Personal name



Funding Source

Organization

None

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

Mitsui Memorial Hospital

Address

Kandaizumicho 1, Chiyoda-ku, Tokyo

Tel

0338629111

Email

ttanaka@mitsuihosp.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

2018 Year 08 Month 15 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

Open public recruiting

Date of protocol fixation

2018 Year 07 Month 05 Day

Date of IRB

2018 Year 07 Month 01 Day

Anticipated trial start date

2018 Year 08 Month 16 Day

Last follow-up date

2023 Year 09 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2018 Year 08 Month 12 Day

Last modified on

2020 Year 02 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000038459


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name