UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000023694
Receipt number R000027287
Scientific Title C-MAC videolaryngoscope versus Macintosh laryngoscope for tracheal intubation: a systematic review and meta-analysis
Date of disclosure of the study information 2017/05/01
Last modified on 2018/08/21 10:02:29

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Basic information

Public title

C-MAC videolaryngoscope versus Macintosh laryngoscope for tracheal intubation: a systematic review and meta-analysis

Acronym

C-MAC videolaryngoscope versus Macintosh laryngoscope for tracheal intubation: a systematic review and meta-analysis

Scientific Title

C-MAC videolaryngoscope versus Macintosh laryngoscope for tracheal intubation: a systematic review and meta-analysis

Scientific Title:Acronym

C-MAC videolaryngoscope versus Macintosh laryngoscope for tracheal intubation: a systematic review and meta-analysis

Region

Japan


Condition

Condition

Patients of tracheal intubation

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

we performed a systematic review and meta-analysis of several randomized controlled trials (RCT) to compare the usefulness of the C-MAC against that of the Macintosh laryngoscope for tracheal intubation with normal and difficult airways.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Assessed by intubation success rate, intubation time, glottis visualisation and number of external laryngeal manipulation.

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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

General anesthesia, Tracheal intubation

Key exclusion criteria

Pediatric

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hoshijima Hiroshi

Organization

Saitama Medical University Hospital

Division name

Department of Anesthesiology

Zip code


Address

38 Morohongo, Moroyama-machi, Iruma-gun, Saitama, 350-0495, Japan

TEL

049-276-1271

Email

hhoshi@saitama-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hoshijima Hiroshi

Organization

Saitama Medical University Hospital

Division name

Department of Anesthesiology

Zip code


Address

38 Morohongo, Moroyama-machi, Iruma-gun, Saitama, 350-0495, Japan

TEL

049-276-1271

Homepage URL


Email

hhoshi@saitama-med.ac.jp


Sponsor or person

Institute

Saitama Medical University Hospital,

Institute

Department

Personal name



Funding Source

Organization

non

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor

Teikyo University School of Medicine, International University of Health and Welfare,Yokohama City University Graduate School of Medicine, Allegheny Health Network

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

2017 Year 05 Month 01 Day


Related information

URL releasing protocol


Publication of results

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

Completed

Date of protocol fixation

2016 Year 01 Month 01 Day

Date of IRB


Anticipated trial start date

2016 Year 07 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

Not start this study


Management information

Registered date

2016 Year 08 Month 19 Day

Last modified on

2018 Year 08 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027287


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name