UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000055034 |
|---|---|
| Receipt number | R000061898 |
| Scientific Title | Visibility of Video Laryngoscope in High-Illuminance Environment Simulating Outdoor conditions |
| Date of disclosure of the study information | 2024/07/21 |
| Last modified on | 2025/07/01 07:39:27 |
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Basic information
Public title
Visibility of Video Laryngoscope in High-Illuminance Environment Simulating Outdoor conditions
Acronym
Visibility of Video Laryngoscope in High-Illuminance Environment
Scientific Title
Visibility of Video Laryngoscope in High-Illuminance Environment Simulating Outdoor conditions
Scientific Title:Acronym
Visibility of Video Laryngoscope in High-Illuminance Environment
Region
| Japan |
Condition
Condition
Simulation
Classification by specialty
| Anesthesiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To identify the effective measures improving visibility of video laryngoscope in high-illuminance environment
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Evaluation of visibility of video laryngoscope by visual analog scale (VAS)
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Self control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Maneuver |
Interventions/Control_1
Polarized Sunglasses, Screen cleaning
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
| 22 | years-old | <= |
Age-upper limit
| 70 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Anesthesiologists and staffs in the operating room
Key exclusion criteria
Exclusion Criteria: Color Vision Abnormality, Visual Acuity Abnormality, and Regular Sunglass Users in Daily Life
Target sample size
25
Research contact person
Name of lead principal investigator
| 1st name | Satoki |
| Middle name | |
| Last name | Inoue |
Organization
Fukushima Medical University
Division name
Anesthesiology
Zip code
960-1295
Address
1 Hikarigaoka, Fukushima, Fukushima 9601295 Japan
TEL
+81245471111
seninoue@fmu.ac.jp
Public contact
Name of contact person
| 1st name | Satoki |
| Middle name | |
| Last name | Inoue |
Organization
Fukushima Medical university
Division name
Anesthesiology
Zip code
960-1295
Address
1 Hikarigaoka, Fukushima, Fukushima 9601295 Japan
TEL
+81245471111
Homepage URL
seninoue@fmu.ac.jp
Sponsor or person
Institute
Fukushima Medical University
Institute
Department
Personal name
Funding Source
Organization
Fukushima Medical University
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
Not applicable
Address
Not applicable
Tel
Not applicable
Not applicable
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 | 07 | Month | 21 | 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
| 2024 | Year | 04 | Month | 20 | Day |
Date of IRB
| 2024 | Year | 04 | Month | 20 | Day |
Anticipated trial start date
| 2024 | Year | 07 | Month | 21 | Day |
Last follow-up date
| 2025 | Year | 08 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2024 | Year | 07 | Month | 21 | Day |
Last modified on
| 2025 | Year | 07 | Month | 01 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061898
