UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000060689
Receipt number R000068893
Scientific Title Association between anesthesiologists experience and intubation performance using the McGRATH MAC video laryngoscope: A multicenter retrospective observational study
Date of disclosure of the study information 2026/02/16
Last modified on 2026/02/16 22:48:47

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Basic information

Public title

Association between anesthesiologists experience and intubation performance using the McGRATH MAC video laryngoscope: A multicenter retrospective observational study

Acronym

EXPERIENCE-INT Study

Scientific Title

Association between anesthesiologists experience and intubation performance using the McGRATH MAC video laryngoscope: A multicenter retrospective observational study

Scientific Title:Acronym

EXPERIENCE-INT Study

Region

Japan


Condition

Condition

Patients who participated in the following study and provided consent for secondary use of their samples and information:

Study title:Examining the intubation complications of different glottal elevation techniques using the McGRATH MAC videolaryngoscope.: A multicentre randomized controlled trial

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the impact of anesthesiologists years of experience on tracheal intubation performance using the McGRATH MAC video laryngoscope (e.g., glottic visualization, intubation success rate, and intubation time).

To compare intubation performance according to years of experience in order to obtain insights that contribute to the optimization of education and training, as well as the improvement of patient safety.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Intubation Performance with the McGRATH MAC Video Laryngoscope According to Anesthesiologists Years of Experience

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

18 years-old <=

Age-upper limit

100 years-old >=

Gender

Male and Female

Key inclusion criteria

Elective surgical patients aged 18 years or older who underwent general anesthesia and were enrolled in a multicenter randomized controlled trial investigating intubation-related complications according to different epiglottis lifting techniques using the McGRATH MAC videolaryngoscope, and for whom all required outcome measures were completely recorded.

Key exclusion criteria

Not applicable

Target sample size

1034


Research contact person

Name of lead principal investigator

1st name Aki
Middle name
Last name Hirai

Organization

Wakayama Medical University School of Medicine

Division name

Department of Anesthesiology

Zip code

641-8509

Address

811-1 Kimiidera, Wakayama City, Wakayama

TEL

+81-73-441-0611

Email

akihri@wakayama-med.ac.jp


Public contact

Name of contact person

1st name Aki
Middle name
Last name Hirai

Organization

Wakayama Medical University School of Medicine

Division name

Department of Anesthesiology

Zip code

641-8509

Address

811-1 Kimiidera, Wakayama City, Wakayama

TEL

+81-73-441-0611

Homepage URL


Email

akihri@wakayama-med.ac.jp


Sponsor or person

Institute

Wakayama Medical University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

None

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

Wakayama Medical University Ethics Review Committee

Address

811-1 Kimiidera, Wakayama City, Wakayama

Tel

0734410897

Email

wa-rinri@wakayama-med.ac.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

2026 Year 02 Month 16 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

1034

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

No longer recruiting

Date of protocol fixation

2026 Year 02 Month 06 Day

Date of IRB

2026 Year 02 Month 06 Day

Anticipated trial start date

2026 Year 02 Month 06 Day

Last follow-up date

2028 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Multicenter Retrospective Observational Study


Management information

Registered date

2026 Year 02 Month 16 Day

Last modified on

2026 Year 02 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000068893