UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Completed
Unique ID issued by UMIN UMIN000014440
Receipt No. R000014546
Scientific Title Multicenter Comparison of Early and Late Vascular Responses to Everolimus-eluting cobalt-CHromium Stent and platelet AggregatioN studIeS for TreatMent of Acute Myocardial Infarction Identically DeSigned bare-Metal stent in patients with Acute Myocardial Infarction: MECHANISM-AMI
Date of disclosure of the study information 2014/07/01
Last modified on 2019/03/28

* 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 Multicenter Comparison of Early and Late Vascular Responses to Everolimus-eluting cobalt-CHromium Stent and platelet AggregatioN studIeS
for TreatMent of Acute Myocardial Infarction Identically DeSigned bare-Metal stent in patients with Acute Myocardial Infarction: MECHANISM-AMI
Acronym MECHANISM-AMI
Scientific Title Multicenter Comparison of Early and Late Vascular Responses to Everolimus-eluting cobalt-CHromium Stent and platelet AggregatioN studIeS
for TreatMent of Acute Myocardial Infarction Identically DeSigned bare-Metal stent in patients with Acute Myocardial Infarction: MECHANISM-AMI
Scientific Title:Acronym MECHANISM-AMI
Region
Japan

Condition
Condition Coronary Artery Disease
Classification by specialty
Cardiology
Classification by malignancy Others
Genomic information YES

Objectives
Narrative objectives1 To evaluate early vessel response between current standard drug-eluting stent and bare-metal stent in acute myocardial infarction (AMI) patients by optical coherence tomography (OCT).
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes The percentage of stent strut coverage by OCT at 2-week or 3-months
Key secondary outcomes

Base
Study type

Study design
Basic design Parallel
Randomization Non-randomized
Randomization unit
Blinding Open -no one is blinded
Control Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 2
Purpose of intervention Treatment
Type of intervention
Device,equipment
Interventions/Control_1 Everolimus-eluting Cobalt Cromium Stent(CoCr-EES),2-week OCT
Interventions/Control_2 Everolimus-eluting Cobalt Cromium Stent(CoCr-EES),3 month OCT
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
85 years-old >
Gender Male and Female
Key inclusion criteria - AMI definition is accordance with the third universal definition of ESC /ACCF/ AHA/ WHF Task Force10, detection of a rise and/or fall of cardiac biomarker values [preferably cardiac troponin (cTn) I or T] with at least one value above the 99th percentile upper reference limit (URL) and with at least one of the following:
Symptoms of ischemia.
New or presumed new significant ST-segment-T wave (ST-T) changes or new left bundlebranch block (LBBB).
Development of pathological Q waves in the ECG.
Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality.
Identification of an intracoronary thrombus by angiography or autopsy
Of the AMI patients who met the above definition, the criterial for inclusion is limited to STEMI patients. STEMI is defined as new ST elevation at the J point in at least 2 contiguous leads of equal or greater than2 mm (0.2 mV) in men equal or greater than1.5 mm (0.15 mV) in women in leads V2-V3 and/or of equal or greater than 1 mm (0.1 mV) in other contiguous chest leads or the limb leads
-Patients having at least one de novo lesion in a coronary artery in whom PCI with a DES is indicated.
-Patients aged 20 to less than 85 years at the time of informed consent
-Patients who have provided informed consent written by themselves
-Patients who are able to undergo OCT examinations of the site of stent placement at 2 weeks or 3 months and at 12 months
Key exclusion criteria 1) Patients who are judged incapable of undergoing clinical follow-up 12 months after PCI (Consider also the location of patients' residences)
2) Lack of specific findings of ACS by angiography (Left to the operator's decision.)
3) Shock
4) The culprit lesion is the left main coronary trunk
5) Lesion with the reference vascular diameter less than 2.0mm or not less than 4.5mm by visual evaluation.
6) AMI due to stent thrombosis at prior stented segment.
7) Chronic renal failure with serum creatinine level not less than 2.0mg/dl on hospital visit
8) Patients on hemodialysis
9) Cancer patients whose vital prognosis is expected to be within 2 years.
10) Surgery that requires discontinuation of the antiplatelet agent is scheduled within 3 months.
11) Female patient plan to became pregnant or during pregnancy.
12) Patients who experienced adverse reaction to aspirin or clopidogrel (this shall not apply for patients in whom safety of ticlopidine is confirmed)
Target sample size 100

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Yoshihiro Morino
Organization Iwate Medical University
Division name Division of Cardiology, Department of Internal Medicine
Zip code
Address 19-1 Uchimaru, Morioka, Iwate
TEL 075-751-4255
Email ymorino@iwate-med.ac.jp

Public contact
Name of contact person
1st name
Middle name
Last name Kanako Omiya
Organization The Academic Research Group for Exploring Undiscovered Mechanisms of Cardiovascular Diseases
Division name Department of cardiovascular medicine
Zip code
Address 19-1 Uchimaru, Morioka, Iwate
TEL 019-651-5111
Homepage URL
Email komiya@iwate-med.ac.jp

Sponsor
Institute Iwate Medical University
Institute
Department

Funding Source
Organization Abbott Vascular Japan, Co., Ltd.
DAIICHI SANKYO COMPANY, LIMITED
Organization
Division
Category of Funding Organization Profit organization
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

Other administrative information
Date of disclosure of the study information
2014 Year 07 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
2014 Year 04 Month 22 Day
Date of IRB
2014 Year 02 Month 04 Day
Anticipated trial start date
2014 Year 05 Month 01 Day
Last follow-up date
2017 Year 05 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
2014 Year 07 Month 01 Day
Last modified on
2019 Year 03 Month 28 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014546

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.