UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000021413
Receipt number R000024700
Scientific Title The effect of oral care using a oral care kit and the oral care application on endotracheal intubation patients
Date of disclosure of the study information 2016/03/10
Last modified on 2020/09/11 09:47:11

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Basic information

Public title

The effect of oral care using a oral care kit and the oral care application on endotracheal intubation patients

Acronym

The effect of oral care using a oral care kit and the oral care application on endotracheal intubation patients

Scientific Title

The effect of oral care using a oral care kit and the oral care application on endotracheal intubation patients

Scientific Title:Acronym

The effect of oral care using a oral care kit and the oral care application on endotracheal intubation patients

Region

Japan


Condition

Condition

Patients undergoing intensive care

Classification by specialty

Intensive care medicine Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study was to clarify that the oral care using a oral care kit and the oral care application for intubated patients will keep oral environment cleaner and decrease silent aspiration more than that with running water.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Pharyngeal mucus and sputum by intratracheal aspiration were obtained three times: soon after intubation,5days later and extubation day.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

oral care using a oral care kit and the oral care application Group

Using a oral care kit and the oral care application for oral care.

Interventions/Control_2

Control Group
Usual oral care.

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Patient with cuffed intratracheal tube
Patient with permanent teeth (one or more teeth)
After written consent was obtained from patient or family
Gender is no object.

Key exclusion criteria

Patient with a history of antibacterial drug use within three months of being admitted.
Patient with a history of 5-and more-day hospitalization within three month of being admitted.
Patient with oral disease
Patient with the possibility of gum bleeding by brushing.

Target sample size

240


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Asami Tado

Organization

Yamaguchi University Graduate School of Medicine

Division name

Faculty of Health Science

Zip code


Address

1-1-1 Minami Kogushi, Ube, Yamaguchi

TEL

0836-22-2842

Email

asamik@yamaguchi-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Asami Tado

Organization

Yamaguchi University Graduate School of Medicine

Division name

Faculty of Health Science

Zip code


Address

1-1-1 Minami Kogushi, Ube,Yamaguchi

TEL

0836-22-2842

Homepage URL


Email

asamik@yamaguchi-u.ac.jp


Sponsor or person

Institute

The field of clinical nursing

Institute

Department

Personal name



Funding Source

Organization

Grant-in-Aid for Young Scientists B

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


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

2016 Year 03 Month 10 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

2015 Year 07 Month 17 Day

Date of IRB

2016 Year 03 Month 01 Day

Anticipated trial start date

2016 Year 03 Month 10 Day

Last follow-up date

2019 Year 03 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2018 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2016 Year 03 Month 09 Day

Last modified on

2020 Year 09 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000024700


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name