UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000024138
Receipt number R000027793
Scientific Title Utility of Semi-automatic Intraosseous Device (EZ-IO) as Reported by Pediatric Nurses and Physicians: A Comparison
Date of disclosure of the study information 2016/09/23
Last modified on 2016/09/28 10:02:02

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Basic information

Public title

Utility of Semi-automatic Intraosseous Device (EZ-IO) as Reported by Pediatric Nurses and Physicians: A Comparison

Acronym

Utility of Semi-automatic Intraosseous Device (EZ-IO) as Reported by Pediatric Nurses and Physicians: A Comparison

Scientific Title

Utility of Semi-automatic Intraosseous Device (EZ-IO) as Reported by Pediatric Nurses and Physicians: A Comparison

Scientific Title:Acronym

Utility of Semi-automatic Intraosseous Device (EZ-IO) as Reported by Pediatric Nurses and Physicians: A Comparison

Region

Japan


Condition

Condition

resuscitation

Classification by specialty

Pediatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare the difficulty scale, time to deployment, and success rate in EZ-IO use between pediatric nurses and physicians.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Mean difficulty rate

Key secondary outcomes

Time to deployment and success rate


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

YES

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Each pediatric nurse was individually trained by the study investigator correctly to deploy the EZ-IO. They were then asked to try inserting a needle into the tibia of an infant training model.

Interventions/Control_2

Each pediatric physician was individually trained by the study investigator correctly to deploy the EZ-IO. They were then asked to try inserting a needle into the tibia of an infant training model.

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Medical personnel who had never used the EZ-IO

Key exclusion criteria

Medical personnel who had ever used the EZ-IO

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Motoki Yasuda

Organization

Tokyo Metropolitan Children's Medical Centor

Division name

Division of Pediatric Emergency Medicine

Zip code


Address

2-8-29, Musashidai, Fuchu, Tokyo, Japan

TEL

042-300-5111

Email

fi000168@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Motoki Yasuda

Organization

Tokyo Metropolitan Children's Medical Centor

Division name

Division of Pediatric Emergency Medicine

Zip code


Address

2-8-29, Musashidai, Fuchu, Tokyo, Japan

TEL

042-300-5111

Homepage URL


Email

fi000168@yahoo.co.jp


Sponsor or person

Institute

Division of Pediatric Emergency Medicine, Tokyo Metropolitan Children's Medical Centor

Institute

Department

Personal name



Funding Source

Organization

Others

Organization

Division

Category of Funding Organization

Local Government

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 09 Month 23 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

2016 Year 06 Month 20 Day

Date of IRB


Anticipated trial start date

2016 Year 06 Month 20 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 09 Month 23 Day

Last modified on

2016 Year 09 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027793


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name