UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000009862
Receipt number R000011556
Scientific Title The onset of nasal bleeding and intubation time by the laterality of the nasal cavity as the route of nasotracheal intubation.
Date of disclosure of the study information 2013/01/25
Last modified on 2013/01/25 11:07:03

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Basic information

Public title

The onset of nasal bleeding and intubation time by the laterality of the nasal cavity as the route of nasotracheal intubation.

Acronym

Nasotracheal intubation and nasal blleding

Scientific Title

The onset of nasal bleeding and intubation time by the laterality of the nasal cavity as the route of nasotracheal intubation.

Scientific Title:Acronym

Nasotracheal intubation and nasal blleding

Region

Japan


Condition

Condition

Nasal bleeding

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

When we perform nasotracheal intubation(NTI), it is necessary to insert a tracheal tube through the left or right nasal cavities. However, unless a clear stenosis of nasal cavity is found beforehand, it depends on an anesthesiologist whether to choose either left or right nasal cavity.
Therefore, we investigated the onset of nasal bleeding and intubation time by the laterality of the nasal cavity as the route of the NTI.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Evaluate the ratio of nasal bleeding

Key secondary outcomes

Evaluate the intubation time


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Maneuver

Interventions/Control_1

Intubation through the right nasal cavity

Interventions/Control_2

Intubation through the left nasal cavity

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

16 years-old <=

Age-upper limit

52 years-old >=

Gender

Male and Female

Key inclusion criteria

Between the age 16 and 52 years old

American Society of Anesthesiologists Class 1 or 2

Key exclusion criteria

We ruled out the patients who had narrow nasal cavity previously and had medication likely to induce bleeding.

Target sample size

190


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Boku Aiji

Organization

Osaka University Graduate School of Dentistry

Division name

Department of Dental Anesthesiology

Zip code


Address

1-8, Yamadaoka, Suita,Osaka

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Osaka University Graduate School of Dentistry

Division name

Department of Dental Anesthesiology

Zip code


Address

1-8, Yamadaoka, Suita,Osaka

TEL


Homepage URL


Email



Sponsor or person

Institute

Osaka University Graduate School of Dentistry

Institute

Department

Personal name



Funding Source

Organization

Osaka University Graduate School of Dentistry

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

2013 Year 01 Month 25 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

2011 Year 12 Month 07 Day

Date of IRB


Anticipated trial start date

2011 Year 12 Month 08 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

2013 Year 01 Month 24 Day

Last modified on

2013 Year 01 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011556


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name