UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Enrolling by invitation
Unique ID issued by UMIN UMIN000012851
Receipt No. R000015011
Scientific Title Clinical evaluation of Glidescope, Kingvision and McGRATH for tracheal intubation by experienced anesthesiologists.
Date of disclosure of the study information 2014/01/14
Last modified on 2014/01/14

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title Clinical evaluation of Glidescope, Kingvision and McGRATH for tracheal intubation by experienced anesthesiologists.
Acronym Evaluation of three types of videolaryngoscope for tracheal intubation.
Scientific Title Clinical evaluation of Glidescope, Kingvision and McGRATH for tracheal intubation by experienced anesthesiologists.
Scientific Title:Acronym Evaluation of three types of videolaryngoscope for tracheal intubation.
Region
Japan

Condition
Condition patients scheduled for elective surgeries
Classification by specialty
Anesthesiology
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To compare three types of videolaryngoscopes; Glidescope, Kingvision and McGRATH, in terms of time to intubation (TTI) and the glottic view.
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1 Confirmatory
Trial characteristics_2 Pragmatic
Developmental phase Not applicable

Assessment
Primary outcomes time to intubation, glottic view
Key secondary outcomes

Base
Study type

Study design
Basic design Parallel
Randomization Randomized
Randomization unit Individual
Blinding Single blind -participants are blinded
Control Uncontrolled
Stratification NO
Dynamic allocation NO
Institution consideration Institution is not considered as adjustment factor.
Blocking NO
Concealment Numbered container method

Intervention
No. of arms 3
Purpose of intervention Treatment
Type of intervention
Device,equipment
Interventions/Control_1 Glidescope group: n=30
Interventions/Control_2 Kingvision group: n=30
Interventions/Control_3 McGRATH group: n=30
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 patients undergoing elective surgeries
Key exclusion criteria ASA class 4, history of cervical surgery,Mallampati class 3,4
Target sample size 90

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Naohiro Mori
Organization Showa University Toyosu Hospital
Division name Department of Anesthesiology
Zip code
Address 4-1-18, Toyosu, Koto-ku, Tokyo
TEL 03-3534-1151
Email morimori-namo.8197b7@cap.ocn.ne.jp

Public contact
Name of contact person
1st name
Middle name
Last name Naohiro Mori
Organization Showa University Toyosu Hospital
Division name Department of Anesthesiology
Zip code
Address 4-1-18, Toyosu, Koto-ku, Tokyo
TEL 03-3534-1151
Homepage URL
Email morimori-namo.8197b7@cap.ocn.ne.jp

Sponsor
Institute department of anesthesiology, Showa University Toyosu Hospital
Institute
Department

Funding Source
Organization department of anesthesiology, Showa University Toyosu 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
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 14 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 Enrolling by invitation
Date of protocol fixation
2013 Year 10 Month 24 Day
Date of IRB
Anticipated trial start date
2013 Year 12 Month 01 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
2014 Year 01 Month 14 Day
Last modified on
2014 Year 01 Month 14 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015011

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.