UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053976
Receipt number R000061613
Scientific Title Investigation of clinical availability of new simple tracheal intubation method using brochofibersope
Date of disclosure of the study information 2024/03/30
Last modified on 2024/03/26 20:05:32

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Basic information

Public title

Investigation of clinical availability of new simple tracheal intubation method using brochofibersope

Acronym

Novel tracheal intubation with bronchofiberscope

Scientific Title

Investigation of clinical availability of new simple tracheal intubation method using brochofibersope

Scientific Title:Acronym

Novel tracheal intubation with bronchofiberscope

Region

Japan


Condition

Condition

Patients receiving general anesthesia with tracheal intubation

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Tracheal intubation using bronchoscopy during general anesthesia is an essential technique in patients in which the conventional intubation methods is difficult such as due to mobid obesity or impaired mouth opening coupled with facial fractures. However, aid of bronchoscopy for tracheal intubation is also useful in other usual cases, such as patients with minor mouth opening problems including temporomandibular joint disorder, fragile teeth, and cervical spondylosis. Therefore, bronchoscopy-assisted intubation has a wide range of clinical indications. However, bronchoscopy-aassisted intubation is a difficult procedure for inexperienced anesthesiologists. We have developed a novel device in which a bronchoscopy and a stylet are preassembled in a tracheal tube. By using this device, even inexperienced anesthesiologists can easily perform bronchoscopy-assisted intubation. The purpose of the present study is to examine the usefulness of our novel bronchoscopy-assisted intubation method.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Successful or unsuccessful tracheal intubation and time required for tracheal intubation.

Key secondary outcomes

Airway mucosal injury or other complications related to tracheal intubation.


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

General anesthesia cases after January 2022 at Kishiwada Tokushukai Hospital.

Key exclusion criteria

Emergency surgery cases.
Highly obese cases with BMI over 30.
Cases with complete orifice dysfunction with fracture.
Cases with intraoral bleeding.
Cases with failure to fast before surgery.
Cases with significant deformity of the oral cavity and upper airway.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Masahiko
Middle name
Last name Tsuchiya

Organization

Kishiwada Tokushukai Hospital

Division name

Department of Anesthesia

Zip code

5968522

Address

4-27-1 Kamori-cho, Kishiwada, Osaka, Japan

TEL

+80-72-445-9915

Email

oxymasa@ea.mbn.or.jp


Public contact

Name of contact person

1st name Masahiko
Middle name
Last name Tsuchiya

Organization

Kishiwada Tokushukai Hospital

Division name

Department of Anesthesia

Zip code

5968522

Address

4-27-1 Kamori-cho, Kishiwada, Osaka, Japan

TEL

+80-72-445-9915

Homepage URL


Email

oxymasa@ea.mbn.or.jp


Sponsor or person

Institute

Kishiwada Tokushukai Hospital

Institute

Department

Personal name



Funding Source

Organization

Kishiwada Tokushukai 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

Kishiwada Tokushuka Hospital

Address

4-27-1 Kamori-cho, Kishiwada, Osaka, Japan

Tel

+80-72-445-9915

Email

oxymasa@ea.mbn.or.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

2024 Year 03 Month 30 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

Enrolling by invitation

Date of protocol fixation

2022 Year 01 Month 01 Day

Date of IRB

2023 Year 05 Month 15 Day

Anticipated trial start date

2022 Year 01 Month 01 Day

Last follow-up date

2024 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2024 Year 03 Month 26 Day

Last modified on

2024 Year 03 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000061613


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name