UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000011226
Receipt No. R000013153
Official scientific title of the study Comparison of the success rate of blind intubation through air-Q in sniffing and neutral position
Date of disclosure of the study information 2013/07/18
Last modified on 2018/10/03 (Ver. 2)

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Basic information
Official scientific title of the study Comparison of the success rate of blind intubation through air-Q in sniffing and neutral position
Title of the study (Brief title) Comparison of the success rate of blind intubation through air-Q in different head position
Region
Japan

Condition
Condition intubation
Classification by specialty
Anesthesiology
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 the success rate of intubation with airQ in sniffing and neutral position
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes the success rate of blind intubation
Key secondary outcomes

Base
Study type Interventional

Study design
Basic design Parallel
Randomization Randomized
Randomization unit Individual
Blinding Open -no one is blinded
Control No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment Numbered container method

Intervention
No. of arms 2
Purpose of intervention Treatment
Type of intervention
Device,equipment
Interventions/Control_1 intubation in neutral position
Interventions/Control_2 intubation in sniffing position
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
70 years-old >=
Gender Male and Female
Key inclusion criteria ASA1-2
scheduled elective surgery
general anesthesia
Key exclusion criteria respiratory disease
gastroesophageal reflex disease
morbid obesity
expected difficult airway
pregnancy
Target sample size 39

Research contact person
Name of lead principal investigator Rieko Yamada
Organization Mizonokuchi Hospital, Teikyo University School of Medicine
Division name Anesthesiology
Address 3-8-3Mizonokuchi, Takatsu, Kawasaki
TEL
Email

Public contact
Name of contact person
Organization Mizonokuchi Hospital, Teikyo University
Division name Anesthesiology
Address
TEL
Homepage URL
Email kinorieko@yahoo.co.jp

Sponsor
Institute Mizonokuchi Hospital, Teikyo University Scool of Medicine
Institute
Department

Funding Source
Organization Teikyo University
Organization
Division
Category of Funding Organization Other
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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 07 Month 18 Day

Progress
Recruitment status Completed
Date of protocol fixation
2011 Year 12 Month 10 Day
Anticipated trial start date
2012 Year 04 Month 10 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Related information
URL releasing protocol
Publication of results Published
URL releasing results
Results
Other related information

Management information
Registered date
2013 Year 07 Month 18 Day
Last modified on
2018 Year 10 Month 03 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013153