UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022503
Receipt number R000025930
Scientific Title Assessment of cardiac involvements in rheumatic diseases : Detecting cardiac magnetic resonance imaging and inflammatory biomarker approach
Date of disclosure of the study information 2016/05/27
Last modified on 2016/05/27 19:22:35

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Basic information

Public title

Assessment of cardiac involvements in rheumatic diseases : Detecting cardiac magnetic resonance imaging and inflammatory biomarker approach

Acronym

Assessment of cardiac involvements in rheumatic diseases

Scientific Title

Assessment of cardiac involvements in rheumatic diseases : Detecting cardiac magnetic resonance imaging and inflammatory biomarker approach

Scientific Title:Acronym

Assessment of cardiac involvements in rheumatic diseases

Region

Japan


Condition

Condition

rheumatic disease

Classification by specialty

Clinical immunology Radiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We sought to assess cardiac involvement using a cardiac magnetic resonance imaging approach and to determine its association with disease characteristics in rheumatic diseases patients

Basic objectives2

Others

Basic objectives -Others

relation between inflammatory biomarker and cardiac involvement in rheumatic diseases

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

We explore the association of cardiac MRI abnormalities with rheumatic disease activity and severity measures.

Key secondary outcomes

Association of cardiac involvement, detecting by a cardiac MRI, with inflammatory biomarker


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

80 years-old >

Gender

Male and Female

Key inclusion criteria

patient, diagnosed with rheumatic disease, without cardiac lesions

Key exclusion criteria

Participants were excluded if they had prior self-reported, physician-diagnosed cardiovascular events or procedures, such as myocardial infarction, angioplasty, and congestive heart failure. Diabetes(HbA1c > 6.1 %), hypertension(systolic blood pressure > 140 mmHg and/or diastolic blood pressure > 90 mmHg), dyslipidemia(LDL cholesterol levels > 140 mg/dL, HDL cholesterol levels < 40 mg/dL, triglyceride levels > 150 mg/dL) were excluded. Furthermore, exclusions were patients who were contraindicated of MRI contrast agent, and who couldn't examine MRI e.g. people containing the cardiac pace maker and so on.

Target sample size

132


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kaita Sugiyama

Organization

Nihon University Itabashi Hospital

Division name

rheumatology

Zip code


Address

30-1 Ooyaguchikamimachi Itabashi-ku Tokyo Japan

TEL

03-3972-8111

Email

kaita_sugiyama@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Akiko Hirama

Organization

Nihon University Itabashi Hospital

Division name

rheumatology

Zip code


Address

30-1 Ooyaguchikamimachi Itabashi-ku Tokyo Japan

TEL

03-3972-8111

Homepage URL


Email

kaita_sugiyama@yahoo.co.jp


Sponsor or person

Institute

Nihon University Itabashi Hospital

Institute

Department

Personal name



Funding Source

Organization

Nihon University Itabashi Hospital

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


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

2016 Year 05 Month 27 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

2016 Year 02 Month 05 Day

Date of IRB


Anticipated trial start date

2016 Year 02 Month 05 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

enrolling by invitation


Management information

Registered date

2016 Year 05 Month 27 Day

Last modified on

2016 Year 05 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025930


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name