UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012854
Receipt number R000015019
Scientific Title Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?
Date of disclosure of the study information 2014/01/15
Last modified on 2014/11/20 13:01:59

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Basic information

Public title

Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?

Acronym

Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?

Scientific Title

Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?

Scientific Title:Acronym

Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?

Region

Japan


Condition

Condition

lung cancer, pneumothorax

Classification by specialty

Chest surgery Anesthesiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Our purpose is to investigate whether we can predict the appropriate insertion depth for a double-lumen endotracheal tube by patient height.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Correlation between patient height and insertion depth for each gender

Key secondary outcomes

Correlation between patient height and insertion depth for both male and female patients


Base

Study type

Others,meta-analysis etc


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who underwent thoracic surgery with a left double-lumen endotracheal tube

Key exclusion criteria

Patients were excluded when one-lung ventilation was not performed properly.

Target sample size

412


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name MASATO SATO

Organization

Keiyu Hospital

Division name

Department of Anesthesiology

Zip code


Address

3-7-3 Minatomirai Nishiku Yokohama Japan

TEL

045-221-8181

Email

keiyumasui@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name MASATO SATO

Organization

Keiyu Hospital

Division name

Department of Anesthesiology

Zip code


Address

3-7-3 Minatomirai Nishiku Yokohama Japan

TEL

045-221-8181

Homepage URL


Email

keiyumasui@gmail.com


Sponsor or person

Institute

Keiyu Hospital

Institute

Department

Personal name



Funding Source

Organization

Keiyu 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

2014 Year 01 Month 15 Day


Related information

URL releasing protocol


Publication of results

Partially published


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 15 Day

Date of IRB


Anticipated trial start date

2014 Year 01 Month 15 Day

Last follow-up date

2014 Year 11 Month 20 Day

Date of closure to data entry

2014 Year 11 Month 20 Day

Date trial data considered complete

2014 Year 11 Month 20 Day

Date analysis concluded

2014 Year 11 Month 20 Day


Other

Other related information

This retrospective study included 412 adult patients (287 men and 125 women) undergoing thoracic surgery with a left-sided double-lumen endotracheal tube.


Management information

Registered date

2014 Year 01 Month 15 Day

Last modified on

2014 Year 11 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015019


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name