UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012930
Receipt number R000015121
Scientific Title Examination of the usefulness of ultrasound-guided central venous catheterization.
Date of disclosure of the study information 2014/01/23
Last modified on 2014/01/23 13:04:22

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Basic information

Public title

Examination of the usefulness of ultrasound-guided central venous catheterization.

Acronym

Examination of the usefulness of ultrasound-guided central venous catheterization.

Scientific Title

Examination of the usefulness of ultrasound-guided central venous catheterization.

Scientific Title:Acronym

Examination of the usefulness of ultrasound-guided central venous catheterization.

Region

Japan


Condition

Condition

Patients scheduled for insertion of a central venous catheter.

Classification by specialty

Medicine in general Surgery in general Obstetrics and Gynecology
Ophthalmology Dermatology Psychiatry
Oto-rhino-laryngology Orthopedics Urology
Neurosurgery Cardiovascular surgery Operative medicine
Intensive care medicine Dental medicine Adult

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safe and reliable central venous catheterization with use of ultrasound.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Puncture site and angle.

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

Adult patients scheduled for insertion of a central venous catheter.

Key exclusion criteria

Child patients, and the one that has an operation career or infection in the puncture site.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shuto Harada

Organization

Asahikawa Medical University

Division name

Department of Anesthesiology and Critical care.

Zip code


Address

Midorigaoka-higashi 2-1-1-1, Asahikawa, Hokkaido, Japan

TEL

0166-68-2583

Email

shootha@asahikawa-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Harada Shuto

Organization

Asahikawa Medical University

Division name

Department of Anesthesiology and Critical care.

Zip code


Address

Midorigaoka-higashi 2-1-1-1, Asahikawa, Hokkaido, Japan

TEL

016-68-2583

Homepage URL


Email

shootha@asahikawa-med.ac.jp


Sponsor or person

Institute

Asahikawa Medical University

Institute

Department

Personal name



Funding Source

Organization

Department of Anesthesiology&Critical care, Asahikawa Medical College

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


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 01 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

Preinitiation

Date of protocol fixation

2014 Year 01 Month 23 Day

Date of IRB


Anticipated trial start date

2014 Year 01 Month 27 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Comparison of puncture site and angle, between a linear probe(pre-scan) and other probe(actual puncture).


Management information

Registered date

2014 Year 01 Month 23 Day

Last modified on

2014 Year 01 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015121


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name