UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040119
Receipt number R000045744
Scientific Title Assessment of distal radial arterial appearance after distal transradial intervention: An intravascular ultrasound study. (ADRENALINE trial)
Date of disclosure of the study information 2020/04/10
Last modified on 2020/04/10 08:40:28

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Basic information

Public title

Assessment of distal radial arterial appearance after distal transradial intervention: An intravascular ultrasound study. (ADRENALINE trial)

Acronym

Assessment of distal radial arterial appearance after DRI using IVUS.

Scientific Title

Assessment of distal radial arterial appearance after distal transradial intervention: An intravascular ultrasound study. (ADRENALINE trial)

Scientific Title:Acronym

Assessment of distal radial arterial appearance after DRI using IVUS.

Region

Japan


Condition

Condition

Ischemic heart disease

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Distal radial artery has been recently used as vascular route for coronary intervention. However, little is known regarding the distal radial artery appearance after distal transradial intervention. The aim of this study is to investigate the distal radial artery after DRI using IVUS.

Basic objectives2

Others

Basic objectives -Others

no description

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The primary endpoint is to assess the distal radial arterial appearance using IVUS

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

IVUS catheter is inserted through the sheath, and placed at the radial artery ostium. The sheath is extracted to a point of 1cm proximal to the puncture point. Automated pull back(1mm/s) imaging is performed to examine the overall radial to distal radial artery.

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

95 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients with ischemic heart disease who are planned to undergo distal radial PCI using IVUS.

Key exclusion criteria

We excluded patients with abnormal Allen test

Target sample size

300


Research contact person

Name of lead principal investigator

1st name Takatoshi
Middle name
Last name Wakeyama

Organization

Japan Community Healthcare Organization Tokuyama Central Hospital

Division name

Division of Cardiology

Zip code

745-8522

Address

1-1, Kodachou, Shunan, Yamaguchi, Japan

TEL

+81-834-28-4411

Email

wakeyama@icloud.com


Public contact

Name of contact person

1st name Takatoshi
Middle name
Last name Wakeyama

Organization

Japan Community Healthcare Organization Tokuyama Central Hospital

Division name

Division of Cardiology

Zip code

745-8522

Address

1-1, Kodachou, Shunan, Yamaguchi, Japan

TEL

+81-834-28-4411

Homepage URL


Email

wakeyama@icloud.com


Sponsor or person

Institute

Japan Community Healthcare Organization Tokuyama Central Hospital

Institute

Department

Personal name



Funding Source

Organization

Japan Community Healthcare Organization Tokuyama Central Hospital

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tokuyama Central Hospital Ethics Committee

Address

1-1, Kodachou, Shunan, Yamaguchi, Japan

Tel

+81-834-28-4411

Email

irb-cr@tokuyama.jcho.go.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

2020 Year 04 Month 10 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

2020 Year 02 Month 01 Day

Date of IRB

2020 Year 02 Month 05 Day

Anticipated trial start date

2020 Year 02 Month 06 Day

Last follow-up date

2023 Year 12 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

2020 Year 04 Month 09 Day

Last modified on

2020 Year 04 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045744