UMIN-CTR Clinical Trial

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

Name:
UMIN ID:

Recruitment status Completed
Unique ID issued by UMIN UMIN000040231
Receipt No. R000045893
Scientific Title Can oral feeding tubes reduce the incidence of ventilator-associated pneumonia compared to nasal feeding tubes in intensive care unit?
Date of disclosure of the study information 2020/04/26
Last modified on 2020/07/08

* 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 Can oral feeding tubes reduce the incidence of ventilator-associated pneumonia compared to nasal feeding tubes in intensive care unit?
Acronym Can oral feeding tubes reduce the incidence of ventilator-associated pneumonia compared to nasal feeding tubes in intensive care unit?
Scientific Title Can oral feeding tubes reduce the incidence of ventilator-associated pneumonia compared to nasal feeding tubes in intensive care unit?
Scientific Title:Acronym Can oral feeding tubes reduce the incidence of ventilator-associated pneumonia compared to nasal feeding tubes in intensive care unit?
Region
Japan

Condition
Condition ventilator-associated pneumonia
Classification by specialty
Emergency medicine Intensive care medicine
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 We analyzed whether there were differences in the incidence of ventilator-associated pneumonia (VAP) between oral feeding tubes and nasal feeding tubes in patients with oral tracheal intubation.
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes incidence of ventilator-associated pneumonia
Key secondary outcomes the onset time of ventilator-associated pneumonia

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
16 years-old <=
Age-upper limit

Not applicable
Gender Male and Female
Key inclusion criteria 1. Patients with oral tracheal intubation
2. Patients with insertion of feeding tubes
Key exclusion criteria 1. Patients with tracheal intubation less
than 48 hours
2. Patients under 16 years
3. Patients diagnosed as pneumonia before
tracheal intubation
4. The case that the study was suspended du
e to the subject's convenience
5. The case that we judged inappropriate
Target sample size 60

Research contact person
Name of lead principal investigator
1st name Yosuke
Middle name Minami
Last name Minami
Organization Tokyo Medical University
Division name Department of Emergency and Critical Care Medicine
Zip code 1600023
Address 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo
TEL 03-3342-6111
Email ymngufdream@gmail.com

Public contact
Name of contact person
1st name Yosuke
Middle name Minami
Last name Minami
Organization Tokyo Medical University
Division name Department of Emergency and Critical Care Medicine
Zip code 1600023
Address 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo
TEL 03-3342-6111
Homepage URL
Email ymngufdream@gmail.com

Sponsor
Institute Tokyo Medical University
Institute
Department

Funding Source
Organization Tokyo Medical University
Organization
Division
Category of Funding Organization Other
Nationality of Funding Organization

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

IRB Contact (For public release)
Organization Tokyo Medical University
Address 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo
Tel 03-3342-6111
Email ymngufdream@gmail.com

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
2020 Year 04 Month 26 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 60
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
2018 Year 11 Month 01 Day
Date of IRB
2020 Year 04 Month 25 Day
Anticipated trial start date
2018 Year 11 Month 01 Day
Last follow-up date
2019 Year 10 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information We analyzed whether there were differences in the incidence of ventilator-associated pneumonia (VAP) between oral feeding tubes and nasal feeding tubes in patients with
oral tracheal intubation. This is
retrospective observational study.

Management information
Registered date
2020 Year 04 Month 24 Day
Last modified on
2020 Year 07 Month 08 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045893

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.