UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000025425
Receipt number R000029267
Scientific Title Are Wireless Electronic Stethoscopes Useful for Respiratory Rate Monitoring During Intravenous Sedation?
Date of disclosure of the study information 2017/01/05
Last modified on 2017/12/28 11:21:54

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Basic information

Public title

Are Wireless Electronic Stethoscopes Useful for Respiratory Rate Monitoring During Intravenous Sedation?

Acronym

The study about usefulness of wireless electronic stethoscope

Scientific Title

Are Wireless Electronic Stethoscopes Useful for Respiratory Rate Monitoring During Intravenous Sedation?

Scientific Title:Acronym

The study about usefulness of wireless electronic stethoscope

Region

Japan


Condition

Condition

Tooth loss

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We compared respiration rate using wireless electronic stethoscope (BrescoRR) and respiration rate using sampling tube for CO2(RR) , to determine whether BrescoRR is useful as a ventilation monitor for intravenous sedation.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

BrescoRR

Key secondary outcomes

RR


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

18 years-old <

Age-upper limit

85 years-old >

Gender

Male and Female

Key inclusion criteria

patients of ASA1 or ASA2 scheduled for implant primary surgery at NDU hospital

Key exclusion criteria

1. Patients commonly used psychotropic drugs, anti-psychotic drugs and sleeping pills
2. Obesity(BMI 25 more)
3. Patients administered before surgery the sedative
4. Patients having history of drug allergy

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Katsuhisa Sunada

Organization

The Nippon Dental University, School of Life Dentistry at Tokyo

Division name

Department of Dental Anesthesiology

Zip code


Address

1-9-20 Fujimi Chiyoda-ku, Tokyo 102-8159, Japan

TEL

03-3261-6560

Email

iamkeikooo@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Keiko Morimoto

Organization

The Nippon Dental University, School of Life Dentistry at Tokyo

Division name

Department of Dental Anesthesiology

Zip code


Address

1-9-20 Fujimi Chiyoda-ku, Tokyo 102-8159, Japan

TEL

03-3261-6560

Homepage URL


Email

iamkeikooo@gmail.com


Sponsor or person

Institute

The Nippon Dental University, School of Life Dentistry at Tokyo

Institute

Department

Personal name



Funding Source

Organization

The Nippon Dental University, School of Life Dentistry at Tokyo

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

2017 Year 01 Month 05 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications

https://doi.org/10.1016/j.joms.2017.08.023

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 12 Month 26 Day

Date of IRB


Anticipated trial start date

2017 Year 01 Month 05 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

nothing


Management information

Registered date

2016 Year 12 Month 27 Day

Last modified on

2017 Year 12 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029267


Research Plan
Registered date File name
2017/06/28 BRESCO倫理審査申請書 11.10.doc

Research case data specifications
Registered date File name
2017/06/28 記録用紙.docx

Research case data
Registered date File name
2017/06/28 実験データ.xlsx